Ranitidine
- Product NDC
- 70518-1361
- 11-digit product format
- 705181361
- Labeler code
- 70518
- Product ID
- 70518-1361_9257911e-161d-7a29-e053-2995a90aa16e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ranitidine
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA078542
- Marketing category
- ANDA
- Marketing start
- 2018-08-09
- 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