Metformin Hydrochloride
- Product NDC
- 60505-0260
- 11-digit product format
- 605050260
- Labeler code
- 60505
- Product ID
- 60505-0260_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
- 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
DailyMed Product Concepts#
DailyMed Socrata Ingredients#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 60505-0260-1 | 60505026001 | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (60505-0260-1) | 2011-12-07 | 2022-04-30 | No | No | Current |
| 60505-0260-2 | 60505026002 | 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (60505-0260-2) | 2011-12-07 | 2022-04-30 | No | No | Current |