Metformin Hydrochloride
- Product NDC
- 71610-740
- 11-digit product format
- 716100740
- Labeler code
- 71610
- Product ID
- 71610-740_d32116fd-aecc-47f1-b713-9c6d5cca6f82
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metformin Hydrochloride
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Aphena Pharma Solutions - Tennessee, LLC
- Application
- ANDA078596
- Marketing category
- ANDA
- Marketing start
- 2022-03-31
- Substance
- METFORMIN HYDROCHLORIDE
- Active strength
- 750 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 | Marketing start | Sample | Exclude flag | Status |
|---|
| 71610-740-53 | 71610074053 | 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71610-740-53) | 2023-11-09 | No | No | Historical |
| 71610-740-60 | 71610074060 | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71610-740-60) | 2023-10-04 | No | No | Historical |
| 71610-740-80 | 71610074080 | 180 TABLET, EXTENDED RELEASE in 1 BOTTLE (71610-740-80) | 2023-10-04 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Metformin Hydrochloride | Aphena Pharma Solutions - Tennessee, LLC | 2023-11-09 | HUMAN PRESCRIPTION DRUG LABEL | 2 |