Ranitidine
- Product NDC
- 70518-0093
- 11-digit product format
- 705180093
- Labeler code
- 70518
- Product ID
- 70518-0093_98b3c130-5aba-67f0-e053-2a95a90af0f9
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ranitidine
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA077824
- Marketing category
- ANDA
- Marketing start
- 2016-12-29
- 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