Metformin Hydrochloride
- Product NDC
- 71335-1162
- 11-digit product format
- 713351162
- Labeler code
- 71335
- Product ID
- 71335-1162_f85e6c3c-ff42-46ae-800b-8d7a862816ed
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metformin Hydrochloride
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA076869
- Marketing category
- ANDA
- Marketing start
- 2005-04-01
- Marketing end
- 0000-00-00
- Substance
- METFORMIN HYDROCHLORIDE
- Active strength
- 750 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 |
|---|
| 71335-1162-1 | 71335116201 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1162-1) | 2019-03-27 | 0000-00-00 | No | No | Current |
| 71335-1162-2 | 71335116202 | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1162-2) | 2019-03-27 | 0000-00-00 | No | No | Current |
| 71335-1162-3 | 71335116203 | 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1162-3) | 2019-03-27 | 0000-00-00 | No | No | Current |
| 71335-1162-4 | 71335116204 | 180 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1162-4) | 2019-03-27 | 0000-00-00 | No | No | Current |
| 71335-1162-5 | 71335116205 | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1162-5) | 2019-03-27 | 0000-00-00 | No | No | Current |