METFORMIN HYDROCHLORIDE
- Product NDC
- 63739-702
- 11-digit product format
- 637390702
- Labeler code
- 63739
- Product ID
- 63739-702_32fe2100-b072-4a1c-9b02-564714b58246
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- METFORMIN HYDROCHLORIDE
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- McKesson Corporation dba SKY Packaging
- Application
- ANDA203686
- Marketing category
- ANDA
- Marketing start
- 2014-12-09
- Marketing end
- 0000-00-00
- Substance
- METFORMIN HYDROCHLORIDE
- Active strength
- 850 mg/1
- Pharmacologic classes
- Biguanide [EPC],Biguanides [CS]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- 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 |
|---|
| 63739-702-10 | METFORMIN HYDROCHLORIDE | 10 in 1 BOX, UNIT-DOSE | TABLET, FILM COATED | 10 | | 7 |
| 63739-702-10 | METFORMIN HYDROCHLORIDE | 10 in 1 BLISTER PACK | TABLET, FILM COATED | 10 | | 7 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 63739-702 | METFORMIN HYDROCHLORIDE TABLET, FILM COATED [MCKESSON CORPORATION DBA SKY PACKAGING] | 7 | Legacy NDC, 2 package rows | 20201113_52e1acef-400d-4d84-9bb8-4d795faa535c.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 63739-702-10 | 63739070210 | 10 in 1 BOX, UNIT-DOSE | Historical |