METFORMIN HYDROCHLORIDE
- Product NDC
- 53808-0713
- 11-digit product format
- 538080713
- Labeler code
- 53808
- Product ID
- 53808-0713_b01de40c-1f85-4255-bcf2-31540bca206a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- METFORMIN HYDROCHLORIDE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- State of Florida DOH Central Pharmacy
- Application
- ANDA075967
- Marketing category
- ANDA
- Marketing start
- 2009-07-01
- Marketing end
- 0000-00-00
- Substance
- METFORMIN HYDROCHLORIDE
- Active strength
- 1000 mg/1
- Pharmacologic classes
- Biguanide [EPC],Biguanides [CS]
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- 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 |
|---|
| 53808-0713-1 | METFORMIN HYDROCHLORIDE | 30 in 1 BLISTER PACK | TABLET | 30 | | 2 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 53808-0713 | METFORMIN HYDROCHLORIDE TABLET METFORMIN HYDROCHLORIDE (METFORMIN HYDROCHLORIDE ) TABLET [STATE OF FLORIDA DOH CENTRAL PHARMACY] | 2 | Legacy NDC, 1 package rows | 20100324_f0a43cae-0f19-4a60-8a82-895cc4ea0001.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 53808-0713-1 | 53808071301 | 30 in 1 BLISTER PACK | Historical |