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Drug Shortages
Drug Shortages

Drug Shortages reported to us

Drug Shortages can occur because of manufacturing and quality problems, delays and discontinuations.


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Drug Shortages

Thursday, September 4, 2025

  • FDA Azelastine Hydrochloride; Fluticasone Propionate Nasal Spray (NDC 00378345823) MYLAN

Wednesday, September 3, 2025

  • MFR Acyclovir 400 MG (NDC 31722077705) CAMBER PHARMACEUTICALS
  • MFR Buprenorphine HCl 8 MG (NDC 00054017713) HIKMA PHARMACEUTICALS USA

Wednesday, August 27, 2025

  • FDA Dobutamine Hydrochloride Injection (NDC 00409234488) HOSPIRA
  • FDA Dopamine Hydrochloride Injection (NDC 00409780924) HOSPIRA

Tuesday, August 19, 2025

  • FDA Finasteride Tablet (NDC 00093735556) TEVA PHARMACEUTICALS USA
  • FDA Finasteride Tablet (NDC 00093735505) TEVA PHARMACEUTICALS USA
  • FDA Finasteride Tablet (NDC 00093735598) TEVA PHARMACEUTICALS USA

Friday, August 15, 2025

  • FDA Celecoxib Capsule (NDC 00591398305) ACTAVIS PHARMA
  • FDA Celecoxib Capsule (NDC 00591398260) ACTAVIS PHARMA
  • FDA Celecoxib Capsule (NDC 00591398401) ACTAVIS PHARMA
  • FDA Celecoxib Capsule (NDC 00591398560) ACTAVIS PHARMA
  • FDA Celecoxib Capsule (NDC 00591398405) ACTAVIS PHARMA
  • FDA Celecoxib Capsule (NDC 00591398301) ACTAVIS PHARMA

Wednesday, August 13, 2025

  • FDA Palivizumab Injection (NDC 66658023001) SOBI
  • FDA Palivizumab Injection (NDC 66658023101) SOBI

Tuesday, August 12, 2025

  • FDA Desipramine Hydrochloride Tablet (NDC 23155058101) AVET PHARMACEUTICALS
  • FDA Desipramine Hydrochloride Tablet (NDC 23155057801) AVET PHARMACEUTICALS
  • FDA Desipramine Hydrochloride Tablet (NDC 23155058201) AVET PHARMACEUTICALS
  • FDA Desipramine Hydrochloride Tablet (NDC 23155058001) AVET PHARMACEUTICALS
  • FDA Desipramine Hydrochloride Tablet (NDC 23155057901) AVET PHARMACEUTICALS
  • FDA Desipramine Hydrochloride Tablet (NDC 23155058325) AVET PHARMACEUTICALS

Friday, August 8, 2025

  • FDA Amphotericin B Injection (NDC 57665010141) LEADIANT BIOSCIENCES

Monday, August 4, 2025

  • FDA Irinotecan Hydrochloride Injection (NDC 45963061451) ACTAVIS
  • FDA Irinotecan Hydrochloride Injection (NDC 45963061455) ACTAVIS

Friday, August 1, 2025

  • FDA Clindamycin Phosphate; Benzoyl Peroxide Gel (NDC 00591391668) ACTAVIS PHARMA

Tuesday, July 29, 2025

  • FDA Adefovir Dipivoxil Tablet (NDC 60505394703) APOTEX
  • FDA Esterified Estrogens Tablet (NDC 61570007301) PFIZER U.S.
  • FDA Esterified Estrogens Tablet (NDC 61570007550) PFIZER U.S.
  • FDA Esterified Estrogens Tablet (NDC 61570007401) PFIZER U.S.
  • FDA Esterified Estrogens Tablet (NDC 61570007201) PFIZER U.S.

Monday, July 28, 2025

  • FDA Voriconazole Tablet (NDC 00049317030) PFIZER U.S.

Thursday, July 24, 2025

  • FDA Glipizide Tablet Extended Release (NDC 00049017808) PFIZER U.S.

Wednesday, July 23, 2025

  • FDA Amantadine Hydrochloride Capsule (NDC 00832101550) UPSHER-SMITH
  • FDA Amantadine Hydrochloride Capsule (NDC 00832101500) UPSHER-SMITH
  • FDA Amantadine Hydrochloride Tablet (NDC 00832011103) UPSHER-SMITH
  • FDA Amantadine Hydrochloride Tablet (NDC 00832011150) UPSHER-SMITH
  • FDA Amantadine Hydrochloride Tablet (NDC 00832011100) UPSHER-SMITH
  • FDA Potassium Chloride Tablet Extended Release (NDC 00832532210) UPSHER-SMITH
  • FDA Potassium Chloride Tablet Extended Release (NDC 00245531515) UPSHER-SMITH
  • FDA Potassium Chloride Tablet Extended Release (NDC 00832532311) UPSHER-SMITH
  • FDA Potassium Chloride Tablet Extended Release (NDC 00245531611) UPSHER-SMITH
  • FDA Potassium Chloride Tablet Extended Release (NDC 00245531615) UPSHER-SMITH
  • FDA Potassium Chloride Tablet Extended Release (NDC 00245531511) UPSHER-SMITH
  • FDA Potassium Chloride Tablet Extended Release (NDC 00245531501) UPSHER-SMITH
  • FDA Potassium Chloride Tablet Extended Release (NDC 00832532211) UPSHER-SMITH
  • FDA Potassium Chloride Tablet Extended Release (NDC 00832532310) UPSHER-SMITH
  • FDA Potassium Chloride Tablet Extended Release (NDC 00245531601) UPSHER-SMITH

Monday, July 21, 2025

  • FDA Insulin Aspart Injection (NDC 73070010315) NOVO NORDISK PHARMA
  • FDA Insulin Aspart Injection (NDC 73070010215) NOVO NORDISK PHARMA
  • FDA Insulin Aspart Injection (NDC 73070010011) NOVO NORDISK PHARMA
  • FDA Insulin Aspart Protamine and Insulin Aspart Mix 70/30 Inject (NDC 73070020315) NOVO NORDISK PHARMA
  • FDA Insulin Aspart Protamine and Insulin Aspart Mix 70/30 Inject (NDC 73070020011) NOVO NORDISK PHARMA
  • FDA Insulin Degludec Injection (NDC 73070050315) NOVO NORDISK PHARMA
  • FDA Insulin Degludec Injection (NDC 73070040315) NOVO NORDISK PHARMA
  • FDA Insulin Degludec Injection (NDC 73070040011) NOVO NORDISK PHARMA

Thursday, July 17, 2025

  • FDA Lidocaine Patch (NDC 00591267930) NOVAPLUS/ACTAVIS
  • FDA Oxaprozin Tablet (NDC 00025138131) PFIZER U.S.
  • FDA Pemetrexed Ditromethamine Injection (NDC 00409106001) HOSPIRA
  • FDA Pemetrexed Ditromethamine Injection (NDC 00409106101) HOSPIRA
  • FDA Potassium Citrate Tablet Extended Release (NDC 00591268201) ACTAVIS PHARMA
  • FDA Potassium Citrate Tablet Extended Release (NDC 00591272901) ACTAVIS PHARMA
  • FDA Potassium Citrate Tablet Extended Release (NDC 00591274201) ACTAVIS PHARMA

Wednesday, July 16, 2025

  • FDA Ethionamide Tablet (NDC 00008411701) PFIZER U.S.

Thursday, July 10, 2025

  • FDA Levothyroxine Sodium Tablet (NDC 72305002530) PROVELL PHARMACEUTICALS
  • FDA Levothyroxine Sodium Tablet (NDC 72305002590) PROVELL PHARMACEUTICALS
  • FDA Levothyroxine Sodium Tablet (NDC 72305005030) PROVELL PHARMACEUTICALS
  • FDA Levothyroxine Sodium Tablet (NDC 72305005090) PROVELL PHARMACEUTICALS
  • FDA Levothyroxine Sodium Tablet (NDC 72305007530) PROVELL PHARMACEUTICALS
  • FDA Levothyroxine Sodium Tablet (NDC 72305007590) PROVELL PHARMACEUTICALS
  • FDA Levothyroxine Sodium Tablet (NDC 72305008830) PROVELL PHARMACEUTICALS
  • FDA Levothyroxine Sodium Tablet (NDC 72305008890) PROVELL PHARMACEUTICALS
  • FDA Levothyroxine Sodium Tablet (NDC 72305010030) PROVELL PHARMACEUTICALS
  • FDA Levothyroxine Sodium Tablet (NDC 72305010090) PROVELL PHARMACEUTICALS
  • FDA Levothyroxine Sodium Tablet (NDC 72305011230) PROVELL PHARMACEUTICALS
  • FDA Levothyroxine Sodium Tablet (NDC 72305011290) PROVELL PHARMACEUTICALS
  • FDA Levothyroxine Sodium Tablet (NDC 72305012530) PROVELL PHARMACEUTICALS
  • FDA Levothyroxine Sodium Tablet (NDC 72305012590) PROVELL PHARMACEUTICALS
  • FDA Levothyroxine Sodium Tablet (NDC 72305013730) PROVELL PHARMACEUTICALS
  • FDA Levothyroxine Sodium Tablet (NDC 72305013790) PROVELL PHARMACEUTICALS
  • FDA Levothyroxine Sodium Tablet (NDC 72305015030) PROVELL PHARMACEUTICALS
  • FDA Levothyroxine Sodium Tablet (NDC 72305015090) PROVELL PHARMACEUTICALS
  • FDA Levothyroxine Sodium Tablet (NDC 72305017530) PROVELL PHARMACEUTICALS
  • FDA Levothyroxine Sodium Tablet (NDC 72305017590) PROVELL PHARMACEUTICALS
  • FDA Levothyroxine Sodium Tablet (NDC 72305020030) PROVELL PHARMACEUTICALS
  • FDA Levothyroxine Sodium Tablet (NDC 72305020090) PROVELL PHARMACEUTICALS

Tuesday, July 8, 2025

  • FDA Morphine Sulfate Injection (NDC 00409189123) HOSPIRA
  • FDA Morphine Sulfate Injection (NDC 00409189201) HOSPIRA
  • FDA Morphine Sulfate Injection (NDC 00409189301) HOSPIRA
  • FDA Oseltamivir Phosphate Capsule (NDC 00004080285) GENENTECH

Important:   Items shown in shortage are based on information provided by wholesalers when they list manufacturer out and discontinued items. Items are shown for 60 days from date of initial insertion on this list.

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