METFORMIN HYDROCHLORIDE
- Product NDC
- 72789-409
- 11-digit product format
- 727890409
- Labeler code
- 72789
- Product ID
- 72789-409_48334c7e-36f3-00ff-e063-6394a90a3f42
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- metformin hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Application
- ANDA213320
- Marketing category
- ANDA
- Marketing start
- 2023-01-19
- Marketing end
- 2027-03-31
- Substance
- METFORMIN HYDROCHLORIDE
- Active strength
- 850 mg/1
- Pharmacologic classes
- Biguanide [EPC], Biguanides [CS]
- NDC exclude flag
- No
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- METFORMIN HYDROCHLORIDE
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| METFORMIN HYDROCHLORIDE | 850 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 786Z46389E |
| Rxcui | 861010 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 72789-409-90 | METFORMIN HYDROCHLORIDE | 90 in 1 BOTTLE, PLASTIC | TABLET | 90 | | 6 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72789-409 | METFORMIN HYDROCHLORIDE TABLET [PD-RX PHARMACEUTICALS, INC.] | 4 | Current NDC, 1 package rows | 20240608_e3e9b582-fd15-4fe0-a210-398d9149696e.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 72789-409-90 | 72789040990 | 90 TABLET in 1 BOTTLE, PLASTIC (72789-409-90) | 90 tablet | 2024-06-07 | 2027-03-31 | No | No | Historical |