Ranitidine
- Product NDC
- 57910-404
- 11-digit product format
- 579100404
- Labeler code
- 57910
- Product ID
- 57910-404_8b783df6-fc22-4128-9cd9-79637a17f97b
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Ranitidine
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Shasun Pharmaceuticals Limited
- Application
- ANDA200536
- Marketing category
- ANDA
- Marketing start
- 2011-06-28
- Marketing end
- 0000-00-00
- Substance
- RANITIDINE HYDROCHLORIDE
- Active strength
- 150 mg/1
- NDC exclude flag
- E
- Listing certified through
- 2018-12-31
- Current FDA listing
- Historical FDA.report record