Ranitidine
- Product NDC
- 62980-514
- 11-digit product format
- 629800514
- Labeler code
- 62980
- Product ID
- 62980-514_66489df3-56c1-4b61-b8a4-f8c2a49f4341
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ranitidine
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Vivimed Labs Limited
- Application
- ANDA210010
- Marketing category
- ANDA
- Marketing start
- 2019-04-01
- Marketing end
- 0000-00-00
- Substance
- RANITIDINE HYDROCHLORIDE
- Active strength
- 150 mg/1
- Pharmacologic classes
- Histamine H2 Receptor Antagonists [MoA],Histamine-2 Receptor Antagonist [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record