Metformin hydrochloride
- Product NDC
- 50742-154
- 11-digit product format
- 507420154
- Labeler code
- 50742
- Product ID
- 50742-154_70359e5d-2824-46ad-8fe0-253272b5ddb9
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metformin hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Ingenus Pharmaceuticals, LLC
- Application
- ANDA090564
- Marketing category
- ANDA
- Marketing start
- 2014-07-16
- Marketing end
- 2022-02-28
- Substance
- METFORMIN HYDROCHLORIDE
- Active strength
- 500 mg/1
- Pharmacologic classes
- Biguanide [EPC],Biguanides [CS]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- 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 |
|---|
| 50742-154-01 | 50742015401 | 100 TABLET, FILM COATED in 1 BOTTLE (50742-154-01) | 2014-07-16 | 2022-02-28 | No | No | Current |
| 50742-154-05 | 50742015405 | 500 TABLET, FILM COATED in 1 BOTTLE (50742-154-05) | 2014-07-16 | 2022-02-28 | No | No | Current |
| 50742-154-10 | 50742015410 | 1000 TABLET, FILM COATED in 1 BOTTLE (50742-154-10) | 2014-07-16 | 2022-02-28 | No | No | Current |
| 50742-154-90 | 50742015490 | 90 TABLET, FILM COATED in 1 BOTTLE (50742-154-90) | 2014-07-16 | 2022-02-28 | No | No | Current |