METFORMIN HYDROCHLORIDE
- Product NDC
- 66064-1041
- 11-digit product format
- 660641041
- Labeler code
- 66064
- Product ID
- 66064-1041_a600530d-9201-4ccc-b677-fc4ecdf7dba7
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- metformin hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Harman Finochem Limited
- Application
- ANDA213320
- Marketing category
- ANDA
- Marketing start
- 2022-06-01
- Marketing end
- 0000-00-00
- Substance
- METFORMIN HYDROCHLORIDE
- Active strength
- 850 mg/1
- Pharmacologic classes
- Biguanide [EPC], Biguanides [CS]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 66064-1041-5 | 66064104105 | 100 AEROSOL in 1 BOTTLE (66064-1041-5) | 100 aerosol | 2022-06-01 | 0000-00-00 | No | No | Current |
| 66064-1041-6 | 66064104106 | 500 AEROSOL in 1 BOTTLE (66064-1041-6) | 500 aerosol | 2022-06-01 | 0000-00-00 | No | No | Current |