Metformin Hydrochloride
- Product NDC
- 48792-7862
- 11-digit product format
- 487927862
- Labeler code
- 48792
- Product ID
- 48792-7862_833c5e2e-8b2d-3b8f-e053-2a91aa0ab453
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metformin Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Sunshine Lake Pharma Co., Ltd.
- Application
- ANDA208999
- Marketing category
- ANDA
- Marketing start
- 2019-03-06
- Marketing end
- 0000-00-00
- Substance
- METFORMIN HYDROCHLORIDE
- Active strength
- 850 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 |
|---|
| 48792-7862-1 | 48792786201 | 100 TABLET, FILM COATED in 1 BOTTLE (48792-7862-1) | 2019-03-06 | 0000-00-00 | No | No | Current |