Metformin Hydrochloride
- Product NDC
- 55154-6296
- 11-digit product format
- 551546296
- Labeler code
- 55154
- Product ID
- 55154-6296_390300c0-29bc-4cda-a76f-95e5ce0632c1
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- metformin hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Cardinal Health
- Application
- ANDA075973
- Marketing category
- ANDA
- Marketing start
- 2012-12-14
- 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 |
|---|
| 55154-6296-0 | 55154629600 | 10 BLISTER PACK in 1 BAG (55154-6296-0) > 1 TABLET, FILM COATED in 1 BLISTER PACK | 10 blister pack | 2012-12-14 | 2021-03-31 | No | No | Current |