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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, July 24, 2025

  • FDA Glucatrol XL Tablet Extended Release 10 mg tablets; bottle o (NDC 00049017808) PFIZER U.S.

Wednesday, July 23, 2025

  • FDA Amantadine Hydrochloride Capsule 100 mg (NDC 00832101550) UPSHER-SMITH
  • FDA Amantadine Hydrochloride Capsule 100 mg (NDC 00832101500) UPSHER-SMITH
  • FDA Amantadine Hydrochloride Tablet 100 mg (NDC 00832011103) UPSHER-SMITH
  • FDA Amantadine Hydrochloride Tablet 100 mg (NDC 00832011150) UPSHER-SMITH
  • FDA Amantadine Hydrochloride Tablet 100 mg (NDC 00832011100) UPSHER-SMITH
  • FDA Klor-Con Tablet Extended Release 600 mg (NDC 00245531515) UPSHER-SMITH
  • FDA Klor-Con Tablet Extended Release 600 mg (NDC 00245531511) UPSHER-SMITH
  • FDA Klor-Con Tablet Extended Release 600 mg (NDC 00245531501) UPSHER-SMITH
  • FDA Klor-Con Tablet Extended Release 750 mg (NDC 00245531601) UPSHER-SMITH
  • FDA Klor-Con Tablet Extended Release 750 mg (NDC 00245531615) UPSHER-SMITH
  • FDA Klor-Con Tablet Extended Release 750 mg (NDC 00245531611) UPSHER-SMITH
  • FDA Potassium Chloride Tablet Extended Release 600 mg (NDC 00832532210) UPSHER-SMITH
  • FDA Potassium Chloride Tablet Extended Release 600 mg (NDC 00832532211) UPSHER-SMITH
  • FDA Potassium Chloride Tablet Extended Release 750 mg (NDC 00832532310) UPSHER-SMITH
  • FDA Potassium Chloride Tablet Extended Release 750 mg (NDC 00832532311) UPSHER-SMITH

Monday, July 21, 2025

  • FDA Insulin Aspart Injection 3 mL Insulin Aspart FlexPen@ (NDC 73070010315) NOVO NORDISK PHARMA
  • FDA Insulin Aspart Injection 3 mL Insulin Aspart PenFill@ cartri (NDC 73070010215) 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 3 mL Insulin Degludec 100 units/m (NDC 73070040315) NOVO NORDISK PHARMA
  • FDA Insulin Degludec Injection 3 mL Insulin Degludec 200 units/m (NDC 73070050315) NOVO NORDISK PHARMA

Thursday, July 17, 2025

  • FDA Daypro Tablet 600 mg (NDC 00025138131) PFIZER U.S.
  • FDA Lidocaine Patch 5% (NDC 00591267930) NOVAPLUS/ACTAVIS
  • FDA Pemetrexed Ditromethamine Injection 100 mg Single Dose Vial (NDC 00409106001) HOSPIRA
  • FDA Pemetrexed Ditromethamine Injection 500 mg Single Dose Vial (NDC 00409106101) HOSPIRA
  • FDA Potassium Citrate Tablet Extended Release 10 meq (NDC 00591272901) ACTAVIS PHARMA
  • FDA Potassium Citrate Tablet Extended Release 15 meq (NDC 00591274201) ACTAVIS PHARMA
  • FDA Potassium Citrate Tablet Extended Release 5 meq (NDC 00591268201) ACTAVIS PHARMA

Thursday, July 10, 2025

  • FDA Euthyrox Tablet 100 ug (NDC 72305010030) PROVELL PHARMACEUTICALS
  • FDA Euthyrox Tablet 100 ug (NDC 72305010090) PROVELL PHARMACEUTICALS
  • FDA Euthyrox Tablet 112 ug (NDC 72305011230) PROVELL PHARMACEUTICALS
  • FDA Euthyrox Tablet 112 ug (NDC 72305011290) PROVELL PHARMACEUTICALS
  • FDA Euthyrox Tablet 125 ug (NDC 72305012530) PROVELL PHARMACEUTICALS
  • FDA Euthyrox Tablet 125 ug (NDC 72305012590) PROVELL PHARMACEUTICALS
  • FDA Euthyrox Tablet 137 ug (NDC 72305013730) PROVELL PHARMACEUTICALS
  • FDA Euthyrox Tablet 137 ug (NDC 72305013790) PROVELL PHARMACEUTICALS
  • FDA Euthyrox Tablet 150 ug (NDC 72305015030) PROVELL PHARMACEUTICALS
  • FDA Euthyrox Tablet 150 ug (NDC 72305015090) PROVELL PHARMACEUTICALS
  • FDA Euthyrox Tablet 175 ug (NDC 72305017530) PROVELL PHARMACEUTICALS
  • FDA Euthyrox Tablet 175 ug (NDC 72305017590) PROVELL PHARMACEUTICALS
  • FDA Euthyrox Tablet 200 ug (NDC 72305020030) PROVELL PHARMACEUTICALS
  • FDA Euthyrox Tablet 200 ug (NDC 72305020090) PROVELL PHARMACEUTICALS
  • FDA Euthyrox Tablet 25 ug (NDC 72305002530) PROVELL PHARMACEUTICALS
  • FDA Euthyrox Tablet 25 ug (NDC 72305002590) PROVELL PHARMACEUTICALS
  • FDA Euthyrox Tablet 50 ug (NDC 72305005030) PROVELL PHARMACEUTICALS
  • FDA Euthyrox Tablet 50 ug (NDC 72305005090) PROVELL PHARMACEUTICALS
  • FDA Euthyrox Tablet 75 ug (NDC 72305007530) PROVELL PHARMACEUTICALS
  • FDA Euthyrox Tablet 75 ug (NDC 72305007590) PROVELL PHARMACEUTICALS
  • FDA Euthyrox Tablet 88 ug (NDC 72305008830) PROVELL PHARMACEUTICALS
  • FDA Euthyrox Tablet 88 ug (NDC 72305008890) PROVELL PHARMACEUTICALS

Tuesday, July 8, 2025

  • FDA Morphine Sulfate Injection 10 mg/1 mL (NDC 00409189301) HOSPIRA
  • FDA Morphine Sulfate Injection 4 mg/1 mL (NDC 00409189123) HOSPIRA
  • FDA Morphine Sulfate Injection 8 mg/1 mL (NDC 00409189201) HOSPIRA
  • FDA Tamiflu Capsule 30 mg (NDC 00004080285) GENENTECH

Tuesday, July 1, 2025

  • FDA Isoniazid Tablet 300 mg (NDC 64950021703) GENUS LIFESCIENCES
  • FDA Isoniazid Tablet 300 mg (NDC 64950021710) GENUS LIFESCIENCES

Friday, June 27, 2025

  • FDA Ezetimibe Tablet 10 mg (NDC 00591371305) ACTAVIS PHARMA
  • FDA Ezetimibe Tablet 10 mg (NDC 00591371319) ACTAVIS PHARMA
  • FDA Ezetimibe Tablet 10 mg (NDC 00591371330) ACTAVIS PHARMA

Thursday, June 26, 2025

  • FDA Eszopiclone Tablet 1 mg (NDC 00093553756) TEVA PHARMACEUTICALS USA
  • FDA Eszopiclone Tablet 2 mg (NDC 00093553801) TEVA PHARMACEUTICALS USA
  • FDA Eszopiclone Tablet 3 mg (NDC 00093553901) TEVA PHARMACEUTICALS USA

Tuesday, June 24, 2025

  • FDA Lotrel Capsule 10 mg; 20 mg (NDC 00078036405) SANDOZ
  • FDA Lotrel Capsule 10 mg; 40 mg (NDC 00078037905) SANDOZ
  • FDA Lotrel Capsule 5 mg; 10 mg (NDC 00078040505) SANDOZ
  • FDA Lotrel Capsule 5 mg; 20 mg (NDC 00078040605) SANDOZ

Monday, June 16, 2025

  • FDA Ethinyl Estradiol; Etonogestrel Ring .015 mg/1 d; .12 mg/1 d (NDC 00093767902) TEVA PHARMACEUTICALS USA
  • FDA Testosterone Gel; Gel Metered 16.2 mg/1 g (NDC 00591292530) ACTAVIS PHARMA
  • FDA Tobramycin Solution 300 mg/4 mL (NDC 00093375028) TEVA PHARMACEUTICALS USA
  • FDA Tobramycin Solution 300 mg/4 mL (NDC 00093375063) TEVA PHARMACEUTICALS USA
  • FDA Tobramycin Solution 300 mg/5 mL (NDC 00093408563) TEVA PHARMACEUTICALS USA

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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