Ranitidine
- Product NDC
- 68788-6382
- 11-digit product format
- 687886382
- Labeler code
- 68788
- Product ID
- 68788-6382_dd346c8b-bc4c-404b-a92b-2745e36f5cf5
- 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
- 2016-05-04
- 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
- 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 |
|---|
| 68788-6382-0 | 68788638200 | 100 TABLET, FILM COATED in 1 BOTTLE (68788-6382-0) | 2016-05-04 | 0000-00-00 | No | No | Current |
| 68788-6382-1 | 68788638201 | 14 TABLET, FILM COATED in 1 BOTTLE (68788-6382-1) | 2016-05-04 | 0000-00-00 | No | No | Current |
| 68788-6382-3 | 68788638203 | 30 TABLET, FILM COATED in 1 BOTTLE (68788-6382-3) | 2016-05-04 | 0000-00-00 | No | No | Current |
| 68788-6382-6 | 68788638206 | 60 TABLET, FILM COATED in 1 BOTTLE (68788-6382-6) | 2016-05-04 | 0000-00-00 | No | No | Current |
| 68788-6382-9 | 68788638209 | 90 TABLET, FILM COATED in 1 BOTTLE (68788-6382-9) | 2016-05-04 | 0000-00-00 | No | No | Current |