Ranitidine
- Product NDC
- 57910-405
- 11-digit product format
- 579100405
- Labeler code
- 57910
- Product ID
- 57910-405_51d82f41-0f1e-4eef-8410-a0e77598f025
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Ranitidine
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Shasun Pharmaceuticals Limited
- Application
- ANDA201745
- Marketing category
- ANDA
- Marketing start
- 2012-02-29
- Marketing end
- 0000-00-00
- Substance
- RANITIDINE HYDROCHLORIDE
- Active strength
- 75 mg/1
- NDC exclude flag
- E
- Listing certified through
- 2018-12-31
- Current FDA listing
- Historical FDA.report record