METFORMIN HYDROCHLORIDE EXTENDED RELEASE
- Product NDC
- 60760-623
- 11-digit product format
- 607600623
- Labeler code
- 60760
- Product ID
- 60760-623_7abc2154-fe12-5c55-e053-2991aa0aaaa1
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- METFORMIN HYDROCHLORIDE
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- St. Marys Medical Park Pharmacy
- Application
- ANDA090295
- Marketing category
- ANDA
- Marketing start
- 2016-05-12
- 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
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 60760-623-60 | 60760062360 | 60 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (60760-623-60) | 2017-12-18 | 0000-00-00 | No | No | Current |