Metformin Hydrochloride
- Product NDC
- 50090-3088
- 11-digit product format
- 500903088
- Labeler code
- 50090
- Product ID
- 50090-3088_47e596c6-9196-4882-a488-fa5cf56af83c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metformin Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA091184
- Marketing category
- ANDA
- Marketing start
- 2011-01-31
- Marketing end
- 0000-00-00
- Substance
- METFORMIN HYDROCHLORIDE
- Active strength
- 500 mg/1
- Pharmacologic classes
- Biguanide [EPC],Biguanides [CS]
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 50090-3088-0 | Metformin Hydrochloride | 33 in 1 BOX, UNIT-DOSE | TABLET, FILM COATED | 33 | | 4 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-3088 | METFORMIN HYDROCHLORIDE TABLET, FILM COATED [A-S MEDICATION SOLUTIONS] | 4 | Legacy NDC, 1 package rows | 20180607_8749ceb8-183a-4f7d-adb7-088480d3a873.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 50090-3088-0 | 50090308800 | 33 in 1 BOX, UNIT-DOSE | Historical |