Metformin Hydrochloride
- Product NDC
- 16714-938
- 11-digit product format
- 167140938
- Labeler code
- 16714
- Product ID
- 16714-938_af6fd4c6-390c-4925-850c-699594e0d024
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metformin Hydrochloride
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- NorthStar RxLLC
- Application
- ANDA202917
- Marketing category
- ANDA
- Marketing start
- 2019-07-25
- 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
- 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 |
|---|
| 16714-938-01 | 16714093801 | 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (16714-938-01) | 2019-07-25 | 0000-00-00 | No | No | Current |