METFORMIN HYDROCHLORIDE
- Product NDC
- 63629-9146
- 11-digit product format
- 636299146
- Labeler code
- 63629
- Product ID
- 63629-9146_66602d0a-43ba-4d87-9cc8-c2150e763e4e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- METFORMIN HYDROCHLORIDE
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA076756
- Marketing category
- ANDA
- Marketing start
- 2020-08-06
- 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
- 2023-12-31
- 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 |
|---|
| 63629-9146-1 | 63629914601 | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (63629-9146-1) | 2022-01-26 | 0000-00-00 | No | No | Current |