Metformin Hydrochloride
- Product NDC
- 71205-686
- 11-digit product format
- 712050686
- Labeler code
- 71205
- Product ID
- 71205-686_52f70c2b-05fa-4bcc-ac3d-60ed60363ca0
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metformin Hydrochloride
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- ANDA206145
- Marketing category
- ANDA
- Marketing start
- 2018-10-27
- Substance
- METFORMIN HYDROCHLORIDE
- Active strength
- 500 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 |
|---|
| 71205-686-30 | 71205068630 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-686-30) | 2022-08-19 | No | No | Historical |
| 71205-686-60 | 71205068660 | 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-686-60) | 2022-08-19 | No | No | Historical |
| 71205-686-72 | 71205068672 | 120 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-686-72) | 2022-11-10 | No | No | Historical |
| 71205-686-90 | 71205068690 | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-686-90) | 2022-08-19 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Metformin Hydrochloride | Proficient Rx LP | 2022-11-01 | HUMAN PRESCRIPTION DRUG LABEL | 2 |