Ranitidine
- Product NDC
- 50090-1496
- 11-digit product format
- 500901496
- Labeler code
- 50090
- Product ID
- 50090-1496_03597182-8947-4dfd-ac3f-14bc4bf37da3
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ranitidine
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA078542
- Marketing category
- ANDA
- Marketing start
- 2008-11-19
- Marketing end
- 0000-00-00
- Substance
- RANITIDINE HYDROCHLORIDE
- Active strength
- 300 mg/1
- Pharmacologic classes
- Histamine H2 Receptor Antagonists [MoA],Histamine-2 Receptor Antagonist [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-1496-0 | 50090149600 | 15 TABLET, FILM COATED in 1 BOTTLE (50090-1496-0) | 2014-12-05 | 0000-00-00 | No | No | Current |
| 50090-1496-1 | 50090149601 | 30 TABLET, FILM COATED in 1 BOTTLE (50090-1496-1) | 2014-12-05 | 0000-00-00 | No | No | Current |
| 50090-1496-3 | 50090149603 | 100 TABLET, FILM COATED in 1 BOTTLE (50090-1496-3) | 2014-12-05 | 0000-00-00 | No | No | Current |
| 50090-1496-4 | 50090149604 | 90 TABLET, FILM COATED in 1 BOTTLE (50090-1496-4) | 2014-12-05 | 0000-00-00 | No | No | Current |