METFORMIN HYDROCHLORIDE
- Product NDC
- 50090-3543
- 11-digit product format
- 500903543
- Labeler code
- 50090
- Product ID
- 50090-3543_57cfbe01-8d82-49bf-a497-2aca1c5e3049
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- METFORMIN HYDROCHLORIDE
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA203686
- Marketing category
- ANDA
- Marketing start
- 2014-12-09
- 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 |
|---|
| 50090-3543-0 | METFORMIN HYDROCHLORIDE | 33 in 1 BOX, UNIT-DOSE | TABLET, FILM COATED | 33 | | 3 |
| 50090-3543-0 | METFORMIN HYDROCHLORIDE | 1 in 1 BLISTER PACK | TABLET, FILM COATED | 1 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-3543 | METFORMIN HYDROCHLORIDE TABLET, FILM COATED [A-S MEDICATION SOLUTIONS] | 3 | Legacy NDC, 2 package rows | 20180820_54bb8030-8e80-4b38-8deb-89c99d73bf09.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 50090-3543-0 | 50090354300 | 33 in 1 BOX, UNIT-DOSE | Historical |