Metformin Hydrochloride
- Product NDC
- 42806-221
- 11-digit product format
- 428060221
- Labeler code
- 42806
- Product ID
- 42806-221_ac5505c5-6cb7-4918-8eb7-433923ff02ad
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metformin Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Epic Pharma, LLC
- Application
- ANDA075965
- Marketing category
- ANDA
- Marketing start
- 2016-04-01
- Marketing end
- 2023-08-31
- Substance
- METFORMIN HYDROCHLORIDE
- Active strength
- 1000 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 |
|---|
| 42806-221-05 | 42806022105 | 500 TABLET, FILM COATED in 1 BOTTLE (42806-221-05) | 2016-04-01 | 0000-00-00 | No | No | Current |