Famotidine
- Product NDC
- 57451-5065
- 11-digit product format
- 574515065
- Labeler code
- 57451
- Product ID
- 57451-5065_65566771-7db3-4f49-ad00-8b561eade5e4
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Famotidine
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Ipca Laboratories Limited
- Application
- ANDA090283
- Marketing category
- ANDA
- Marketing start
- 2010-06-25
- Marketing end
- 0000-00-00
- Substance
- FAMOTIDINE
- Active strength
- 10 mg/1
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#