METFORMIN HYDROCHLORIDE EXTENDED RELEASE
- Product NDC
- 70934-334
- 11-digit product format
- 709340334
- Labeler code
- 70934
- Product ID
- 70934-334_a720569d-a8ed-48aa-e053-2995a90a5394
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- METFORMIN HYDROCHLORIDE
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Denton Pharma, Inc. DBA Northwind Pharmaceuticals
- Application
- ANDA090295
- Marketing category
- ANDA
- Marketing start
- 2019-04-08
- 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
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70934-334-30 | 70934033430 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70934-334-30) | 2019-04-08 | 0000-00-00 | No | No | Current |