METFORMIN HYDROCHLORIDE
- Product NDC
- 71335-0140
- 11-digit product format
- 713350140
- Labeler code
- 71335
- Product ID
- 71335-0140_1e0f6733-7ec2-47ce-802a-6132a701e1b3
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- METFORMIN HYDROCHLORIDE
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA077336
- Marketing category
- ANDA
- Marketing start
- 2006-02-09
- Marketing end
- 0000-00-00
- Substance
- METFORMIN HYDROCHLORIDE
- Active strength
- 750 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 table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71335-0140-1 | 71335014001 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0140-1) | 2022-01-20 | 0000-00-00 | No | No | Current |
| 71335-0140-2 | 71335014002 | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0140-2) | 2022-01-20 | 0000-00-00 | No | No | Current |
| 71335-0140-3 | 71335014003 | 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0140-3) | 2022-01-20 | 0000-00-00 | No | No | Current |
| 71335-0140-4 | 71335014004 | 180 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0140-4) | 2022-01-20 | 0000-00-00 | No | No | Current |
| 71335-0140-5 | 71335014005 | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0140-5) | 2022-01-20 | 0000-00-00 | No | No | Current |