Metformin Hydrochloride
- Product NDC
- 60505-1329
- 11-digit product format
- 605051329
- Labeler code
- 60505
- Product ID
- 60505-1329_9edce5ce-f627-2898-8fa5-8fb076709ec3
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metformin Hydrochloride
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Apotex Corp.
- Application
- ANDA076706
- Marketing category
- ANDA
- Marketing start
- 2005-12-29
- Marketing end
- 2021-03-31
- Substance
- METFORMIN HYDROCHLORIDE
- Active strength
- 750 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 |
|---|
| 60505-1329-1 | 60505132901 | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (60505-1329-1) | 2011-12-07 | 2021-03-31 | No | No | Current |
| 60505-1329-3 | 60505132903 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (60505-1329-3) | 2011-12-07 | 2021-03-31 | No | No | Current |
| 60505-1329-5 | 60505132905 | 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (60505-1329-5) | 2011-12-07 | 2021-03-31 | No | No | Current |