METFORMIN HYDROCHLORIDE EXTENDED RELEASE
- Product NDC
- 70934-309
- 11-digit product format
- 709340309
- Labeler code
- 70934
- Product ID
- 70934-309_89f4ad27-1d92-7720-e053-2a95a90a4c31
- 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
- 2019-03-07
- 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
- 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 |
|---|
| 70934-309-30 | 70934030930 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70934-309-30) | 2019-08-21 | 0000-00-00 | No | No | Current |
| 70934-309-60 | 70934030960 | 60 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70934-309-60) | 2019-07-02 | 0000-00-00 | No | No | Current |
| 70934-309-90 | 70934030990 | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70934-309-90) | 2019-03-12 | 0000-00-00 | No | No | Current |
| 70934-309-98 | 70934030998 | 120 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70934-309-98) | 2019-03-07 | 0000-00-00 | No | No | Current |