Metformin Hydrochloride
- Product NDC
- 61442-361
- 11-digit product format
- 614420361
- Labeler code
- 61442
- Product ID
- 61442-361_308dc0ee-f470-376f-e054-00144ff88e88
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metformin Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Carlsbad Technology, Inc.
- Application
- ANDA203769
- Marketing category
- ANDA
- Marketing start
- 2014-02-01
- Marketing end
- 0000-00-00
- Substance
- METFORMIN HYDROCHLORIDE
- Active strength
- 500 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 |
|---|
| 61442-361-01 | 61442036101 | 100 TABLET, FILM COATED in 1 BOTTLE (61442-361-01) | 2014-02-01 | 0000-00-00 | No | No | Current |
| 61442-361-05 | 61442036105 | 500 TABLET, FILM COATED in 1 BOTTLE (61442-361-05) | 2014-02-01 | 0000-00-00 | No | No | Current |
| 61442-361-10 | 61442036110 | 1000 TABLET, FILM COATED in 1 BOTTLE (61442-361-10) | 2014-02-01 | 0000-00-00 | No | No | Current |