Metformin hydrochloride
- Product NDC
- 51655-562
- 11-digit product format
- 516550562
- Labeler code
- 51655
- Product ID
- 51655-562_c7ae5667-dab8-42b6-9224-86f284b16536
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metformin hydrochloride ER
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Northwind Pharmaceuticals
- Application
- ANDA076869
- Marketing category
- ANDA
- Marketing start
- 2014-06-01
- 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
- 2019-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 51655-562 | METFORMIN HYDROCHLORIDE ER TABLET [NORTHWIND PHARMACEUTICALS] | 1 | Legacy NDC | 20140619_5909a843-51d7-4cc2-a2ad-b848463e85b6.zip |