smart sense famotidine
- Product NDC
- 49738-201
- 11-digit product format
- 497380201
- Labeler code
- 49738
- Product ID
- 49738-201_1afd815b-6502-41eb-870a-5af70a1e1d14
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Famotidine
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Kmart Corporation
- Application
- ANDA075400
- Marketing category
- ANDA
- Marketing start
- 2014-02-18
- Marketing end
- 0000-00-00
- Substance
- FAMOTIDINE
- Active strength
- 10 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record