Metformin Hydrochloride
- Product NDC
- 35356-886
- 11-digit product format
- 353560886
- Labeler code
- 35356
- Product ID
- 35356-886_d7609164-67b9-4116-a2ef-630d967d5252
- 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
- 2005-01-14
- Marketing end
- 0000-00-00
- Substance
- METFORMIN HYDROCHLORIDE
- Active strength
- 1000 mg/1
- Pharmacologic classes
- Biguanide [EPC],Biguanides [CS]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- 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 |
|---|
| 35356-886-30 | 35356088630 | 30 TABLET, FILM COATED in 1 BOTTLE (35356-886-30) | 2005-01-14 | 0000-00-00 | No | No | Current |