Ranitidine Hydrochloride
- Product NDC
- 68094-204
- 11-digit product format
- 680940204
- Labeler code
- 68094
- Product ID
- 68094-204_e139e59a-e1b0-429c-81b7-7cfc4ea33d76
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ranitidine Hydrochloride
- Dosage form
- SOLUTION
- Route
- ORAL
- Labeler
- Precision Dose Inc.
- Application
- ANDA078312
- Marketing category
- ANDA
- Marketing start
- 2003-08-21
- Marketing end
- 2020-04-30
- Substance
- RANITIDINE HYDROCHLORIDE
- Active strength
- 150 mg/10mL
- Pharmacologic classes
- Histamine H2 Receptor Antagonists [MoA],Histamine-2 Receptor Antagonist [EPC]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record