METFORMIN HYDROCHLORIDE
- Product NDC
- 50090-7588
- 11-digit product format
- 500907588
- Labeler code
- 50090
- Product ID
- 50090-7588_1f71a89a-b3ee-4393-ad40-82553fa628f1
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- METFORMIN HYDROCHLORIDE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA203769
- Marketing category
- ANDA
- Marketing start
- 2015-02-01
- Substance
- METFORMIN HYDROCHLORIDE
- Active strength
- 1000 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 |
|---|
| 50090-7588-0 | 50090758800 | 90 TABLET in 1 BOTTLE (50090-7588-0) | 90 tablet | 2025-06-30 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| METFORMIN HYDROCHLORIDE | A-S Medication Solutions | 2025-07-09 | HUMAN PRESCRIPTION DRUG LABEL | 1 |