Metformin Hydrochloride
- Product NDC
- 66116-378
- 11-digit product format
- 661160378
- Labeler code
- 66116
- Product ID
- 66116-378_5fb922d2-e71b-4f67-847e-92d820ebc3d6
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metformin Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- MedVantx, Inc.
- Application
- ANDA075978
- Marketing category
- ANDA
- Marketing start
- 2010-07-27
- Marketing end
- 0000-00-00
- Substance
- METFORMIN HYDROCHLORIDE
- Active strength
- 500 mg/1
- Pharmacologic classes
- Biguanide [EPC],Biguanides [CS]
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 66116-378-60 | Metformin Hydrochloride | 60 in 1 BOTTLE | TABLET, FILM COATED | 60 | | 1 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 66116-378 | METFORMIN HYDROCHLORIDE TABLET, FILM COATED [MEDVANTX, INC.] | 1 | Legacy NDC, 1 package rows | 20111220_5fb922d2-e71b-4f67-847e-92d820ebc3d6.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 66116-378-60 | 66116037860 | 60 in 1 BOTTLE | Historical |