Metformin Hydrochloride
- Product NDC
- 50090-2173
- 11-digit product format
- 500902173
- Labeler code
- 50090
- Product ID
- 50090-2173_e7cb24db-564c-4cab-9b9a-0f7863a52536
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metformin Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA077095
- Marketing category
- ANDA
- Marketing start
- 2005-01-14
- 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
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 50090-2173-0 | Metformin Hydrochloride | 60 in 1 BOTTLE | TABLET, FILM COATED | 60 | | 38 |
| 50090-2173-2 | Metformin Hydrochloride | 100 in 1 BOTTLE | TABLET, FILM COATED | 100 | | 38 |
| 50090-2173-4 | Metformin Hydrochloride | 90 in 1 BOTTLE | TABLET, FILM COATED | 90 | | 38 |
| 50090-2173-5 | Metformin Hydrochloride | 180 in 1 BOTTLE | TABLET, FILM COATED | 180 | | 38 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-2173 | METFORMIN HYDROCHLORIDE TABLET, FILM COATED [A-S MEDICATION SOLUTIONS] | 27 | Legacy NDC, 4 package rows | 20250516_23aa50c5-28fe-4322-b5c6-1f1c48409b16.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 50090-2173-0 | 50090217300 | 60 in 1 BOTTLE | Historical |
| 50090-2173-2 | 50090217302 | 100 in 1 BOTTLE | Historical |
| 50090-2173-4 | 50090217304 | 90 in 1 BOTTLE | Historical |
| 50090-2173-5 | 50090217305 | 180 in 1 BOTTLE | Historical |