Metformin hydrochloride
- Product NDC
- 51655-550
- 11-digit product format
- 516550550
- Labeler code
- 51655
- Product ID
- 51655-550_fd289a35-1096-43a6-88fe-5bc685961eaa
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metformin hydrochloride
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Northwind Pharmaceuticals
- Application
- ANDA076706
- Marketing category
- ANDA
- Marketing start
- 2014-04-23
- 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
- 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 |
|---|
| 51655-550 | METFORMIN HYDROCHLORIDE ER (METFORMIN HYDROCHLORIDE) TABLET, EXTENDED RELEASE [NORTHWIND PHARMACEUTICALS] | 2 | Legacy NDC | 20141001_c9148dea-a3d1-4134-9287-cb2cf16e3794.zip |