Metformin Hydrochloride
- Product NDC
- 49999-106
- 11-digit product format
- 499990106
- Labeler code
- 49999
- Product ID
- 49999-106_10c01ecc-f50c-4da7-8191-040cc1846048
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metformin Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Lake Erie Medical DBA Quality Care Products LLC
- Application
- ANDA077095
- Marketing category
- ANDA
- Marketing start
- 2011-01-27
- Marketing end
- 0000-00-00
- Substance
- METFORMIN HYDROCHLORIDE
- Active strength
- 500 mg/1
- Pharmacologic classes
- Biguanide [EPC],Biguanides [CS]
- 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 |
|---|
| 49999-106-30 | 49999010630 | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (49999-106-30) | 2011-01-27 | 0000-00-00 | No | No | Current |