Metformin Hydrochloride
- Product NDC
- 71205-372
- 11-digit product format
- 712050372
- Labeler code
- 71205
- Product ID
- 71205-372_0a484822-d247-466c-bd52-2318303870dd
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metformin Hydrochloride
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- ANDA076706
- Marketing category
- ANDA
- Marketing start
- 2004-12-16
- Marketing end
- 2022-04-30
- Substance
- METFORMIN HYDROCHLORIDE
- Active strength
- 500 mg/1
- Pharmacologic classes
- Biguanide [EPC],Biguanides [CS]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- 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 |
|---|
| 71205-372-30 | 71205037230 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-372-30) | 2019-12-13 | 2022-04-30 | No | No | Current |
| 71205-372-60 | 71205037260 | 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-372-60) | 2019-12-13 | 2022-04-30 | No | No | Current |
| 71205-372-90 | 71205037290 | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-372-90) | 2019-12-13 | 2022-04-30 | No | No | Current |