Metformin Hydrochloride
- Product NDC
- 51079-172
- 11-digit product format
- 510790172
- Labeler code
- 51079
- Product ID
- 51079-172_96b16cf3-df7a-9968-e053-2995a90a3b9f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- metformin hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Mylan Institutional Inc.
- Application
- ANDA075973
- Marketing category
- ANDA
- Marketing start
- 2012-08-17
- Marketing end
- 2021-03-31
- 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 | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 51079-172-20 | 51079017220 | 100 BLISTER PACK in 1 CARTON (51079-172-20) > 1 TABLET, FILM COATED in 1 BLISTER PACK (51079-172-01) | 100 blister pack | 2012-08-17 | 2021-03-31 | No | No | Current |