Ranitidine 75
- Product NDC
- 41250-131
- 11-digit product format
- 412500131
- Labeler code
- 41250
- Product ID
- 41250-131_cabe7b1b-4c11-11f3-b279-21d271df7cd1
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Ranitidine Tablets
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Meijer Distribution Inc
- Application
- ANDA075294
- Marketing category
- ANDA
- Marketing start
- 2014-09-22
- Marketing end
- 0000-00-00
- Substance
- RANITIDINE HYDROCHLORIDE
- Active strength
- 75 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record