NDC 0378-3020

Famotidine

Famotidine

Famotidine is a Oral Tablet, Film Coated in the Human Prescription Drug category. It is labeled and distributed by Mylan Pharmaceuticals Inc.. The primary component is Famotidine.

Product ID0378-3020_3d598544-4d57-4875-b685-99a108270be4
NDC0378-3020
Product TypeHuman Prescription Drug
Proprietary NameFamotidine
Generic NameFamotidine
Dosage FormTablet, Film Coated
Route of AdministrationORAL
Marketing Start Date2001-04-16
Marketing End Date2020-02-29
Marketing CategoryANDA / ANDA
Application NumberANDA075704
Labeler NameMylan Pharmaceuticals Inc.
Substance NameFAMOTIDINE
Active Ingredient Strength20 mg/1
Pharm ClassesHistamine H2 Receptor Antagonists [MoA],Histamine-2 Receptor Antagonist [EPC]
NDC Exclude FlagN

Packaging

NDC 0378-3020-05

500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-3020-05)
Marketing Start Date2001-04-16
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 0378-3020-05 [00378302005]

Famotidine TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA075704
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2001-04-16
Marketing End Date2020-02-29

NDC 0378-3020-01 [00378302001]

Famotidine TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA075704
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2001-04-16
Marketing End Date2020-02-29

Drug Details

Pharmacological Class

  • Histamine H2 Receptor Antagonists [MoA]
  • Histamine-2 Receptor Antagonist [EPC]