Metformin HCl
- Product NDC
- 71205-567
- 11-digit product format
- 712050567
- Labeler code
- 71205
- Product ID
- 71205-567_09678d2f-39cd-4821-bcac-3ecdc853f822
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metformin HCl
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- ANDA090564
- Marketing category
- ANDA
- Marketing start
- 2017-02-06
- Substance
- METFORMIN HYDROCHLORIDE
- Active strength
- 850 mg/1
- Pharmacologic classes
- Biguanide [EPC], Biguanides [CS]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 786Z46389E | METFORMIN HYDROCHLORIDE | 1115-70-4 | METFORMIN HYDROCHLORIDE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 71205-567-00 | 71205056700 | 100 TABLET in 1 BOTTLE (71205-567-00) | 100 tablet | 2021-06-23 | No | No | Historical |
| 71205-567-30 | 71205056730 | 30 TABLET in 1 BOTTLE (71205-567-30) | 30 tablet | 2021-05-17 | No | No | Historical |
| 71205-567-60 | 71205056760 | 60 TABLET in 1 BOTTLE (71205-567-60) | 60 tablet | 2021-05-17 | No | No | Historical |
| 71205-567-90 | 71205056790 | 90 TABLET in 1 BOTTLE (71205-567-90) | 90 tablet | 2021-05-17 | No | No | Historical |