METFORMIN HYDROCHLORIDE
- Product NDC
- 70934-399
- 11-digit product format
- 709340399
- Labeler code
- 70934
- Product ID
- 70934-399_b09c90a8-0720-c05f-e053-2a95a90a02e3
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- METFORMIN HYDROCHLORIDE
- Dosage form
- TABLET, COATED
- Route
- ORAL
- Labeler
- Denton Pharma, Inc. DBA Northwind Pharmaceuticals
- Application
- ANDA205096
- Marketing category
- ANDA
- Marketing start
- 2019-06-27
- Marketing end
- 0000-00-00
- Substance
- METFORMIN HYDROCHLORIDE
- Active strength
- 1000 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 |
|---|
| 70934-399-90 | 70934039990 | 90 TABLET, COATED in 1 BOTTLE, PLASTIC (70934-399-90) | 2019-06-27 | 0000-00-00 | No | No | Current |