Metformin Hydrochloride
- Product NDC
- 68788-7889
- 11-digit product format
- 687887889
- Labeler code
- 68788
- Product ID
- 68788-7889_59ab8edd-3099-4b51-b36e-dd4faab288c6
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metformin Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals Inc.
- Application
- ANDA209882
- Marketing category
- ANDA
- Marketing start
- 2021-04-23
- Marketing end
- 0000-00-00
- Substance
- METFORMIN HYDROCHLORIDE
- Active strength
- 1000 mg/1
- Pharmacologic classes
- Biguanide [EPC], Biguanides [CS]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- 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 |
|---|
| 68788-7889-1 | 68788788901 | 100 TABLET, FILM COATED in 1 BOTTLE (68788-7889-1) | 2021-04-23 | 0000-00-00 | No | No | Current |
| 68788-7889-3 | 68788788903 | 30 TABLET, FILM COATED in 1 BOTTLE (68788-7889-3) | 2021-04-23 | 0000-00-00 | No | No | Current |
| 68788-7889-6 | 68788788906 | 60 TABLET, FILM COATED in 1 BOTTLE (68788-7889-6) | 2021-04-23 | 0000-00-00 | No | No | Current |
| 68788-7889-7 | 68788788907 | 180 TABLET, FILM COATED in 1 BOTTLE (68788-7889-7) | 2021-04-23 | 0000-00-00 | No | No | Current |
| 68788-7889-8 | 68788788908 | 120 TABLET, FILM COATED in 1 BOTTLE (68788-7889-8) | 2021-04-23 | 0000-00-00 | No | No | Current |
| 68788-7889-9 | 68788788909 | 90 TABLET, FILM COATED in 1 BOTTLE (68788-7889-9) | 2021-04-23 | 0000-00-00 | No | No | Current |