Famotidine
- Product NDC
- 70934-553
- 11-digit product format
- 709340553
- Labeler code
- 70934
- Product ID
- 70934-553_ac8c65ad-7d6a-1aa1-e053-2995a90a65e2
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Famotidine
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Denton Pharma, Inc. DBA Northwind Pharmaceuticals
- Application
- ANDA078916
- Marketing category
- ANDA
- Marketing start
- 2020-02-14
- Marketing end
- 0000-00-00
- Substance
- FAMOTIDINE
- Active strength
- 40 mg/1
- Pharmacologic classes
- Histamine H2 Receptor Antagonists [MoA],Histamine-2 Receptor Antagonist [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record