Ranitidine
- Product NDC
- 49035-117
- 11-digit product format
- 490350117
- Labeler code
- 49035
- Product ID
- 49035-117_62a8eebf-f563-3cd9-41f3-7ee316267790
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Ranitidine Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Wal-mart Stores Inc
- Application
- ANDA200172
- Marketing category
- ANDA
- Marketing start
- 2017-06-29
- Marketing end
- 2021-01-31
- Substance
- RANITIDINE HYDROCHLORIDE
- Active strength
- 150 mg/1
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record