Ranitidine
- Product NDC
- 68788-7101
- 11-digit product format
- 687887101
- Labeler code
- 68788
- Product ID
- 68788-7101_8c8ed582-230d-4c61-a754-6f14aee9d8b4
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- RANITIDINE
- Dosage form
- SYRUP
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals Inc.
- Application
- ANDA077405
- Marketing category
- ANDA
- Marketing start
- 2018-03-13
- Marketing end
- 0000-00-00
- Substance
- RANITIDINE
- Active strength
- 15 mg/mL
- 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