Famotidine
- Product NDC
- 70518-2469
- 11-digit product format
- 705182469
- Labeler code
- 70518
- Product ID
- 70518-2469_993b9f79-8538-28c2-e053-2a95a90aa900
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Famotidine
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA078916
- Marketing category
- ANDA
- Marketing start
- 2019-12-06
- Marketing end
- 0000-00-00
- Substance
- FAMOTIDINE
- Active strength
- 20 mg/1
- Pharmacologic classes
- Histamine H2 Receptor Antagonists [MoA],Histamine-2 Receptor Antagonist [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record