smart sense ranitidine
- Product NDC
- 49738-361
- 11-digit product format
- 497380361
- Labeler code
- 49738
- Product ID
- 49738-361_3aaf662a-fc5f-4c9d-ac4e-b5c134d207eb
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Ranitidine
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Kmart Corporation
- Application
- ANDA091429
- Marketing category
- ANDA
- Marketing start
- 2014-03-21
- Marketing end
- 0000-00-00
- Substance
- RANITIDINE HYDROCHLORIDE
- Active strength
- 150 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record