METFORMIN HYDROCHLORIDE EXTENDED RELEASE
- Product NDC
- 71335-1310
- 11-digit product format
- 713351310
- Labeler code
- 71335
- Product ID
- 71335-1310_6c8eca76-d80c-4331-a5d2-3103bcacec04
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- METFORMIN HYDROCHLORIDE
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA090295
- Marketing category
- ANDA
- Marketing start
- 2016-05-12
- 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 |
|---|
| 71335-1310-1 | 71335131001 | 180 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1310-1) | 2019-08-26 | 0000-00-00 | No | No | Current |
| 71335-1310-2 | 71335131002 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1310-2) | 2019-08-26 | 0000-00-00 | No | No | Current |