Ranitidine
- Product NDC
- 68788-7388
- 11-digit product format
- 687887388
- Labeler code
- 68788
- Product ID
- 68788-7388_e2cb0452-be57-4083-9f22-ac14cccb58f8
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ranitidine
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals Inc.
- Application
- ANDA078542
- Marketing category
- ANDA
- Marketing start
- 2016-09-16
- 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
- 2021-12-31
- 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 |
|---|
| 68788-7388-1 | 68788738801 | 100 TABLET, FILM COATED in 1 BOTTLE (68788-7388-1) | 2016-09-16 | 0000-00-00 | No | No | Current |
| 68788-7388-3 | 68788738803 | 30 TABLET, FILM COATED in 1 BOTTLE (68788-7388-3) | 2016-09-16 | 0000-00-00 | No | No | Current |
| 68788-7388-6 | 68788738806 | 60 TABLET, FILM COATED in 1 BOTTLE (68788-7388-6) | 2016-09-16 | 0000-00-00 | No | No | Current |
| 68788-7388-8 | 68788738808 | 120 TABLET, FILM COATED in 1 BOTTLE (68788-7388-8) | 2016-09-16 | 0000-00-00 | No | No | Current |
| 68788-7388-9 | 68788738809 | 90 TABLET, FILM COATED in 1 BOTTLE (68788-7388-9) | 2016-09-16 | 0000-00-00 | No | No | Current |