Metformin HCL
- Product NDC
- 72189-658
- 11-digit product format
- 721890658
- Labeler code
- 72189
- Product ID
- 72189-658_4ce98cec-b62c-e8e8-e063-6394a90ac207
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metformin HCL
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Direct_Rx
- Application
- ANDA209882
- Marketing category
- ANDA
- Marketing start
- 2026-01-29
- Substance
- METFORMIN HYDROCHLORIDE
- Active strength
- 500 mg/1
- Pharmacologic classes
- Biguanide [EPC], Biguanides [CS]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Metformin HCL
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| METFORMIN HYDROCHLORIDE | 500 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 786Z46389E |
| Rxcui | 861007 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 72189-658-30 | Metformin HCL | 30 in 1 BOTTLE | TABLET, FILM COATED | 30 | | 3 |
| 72189-658-82 | Metformin HCL | 180 in 1 BOTTLE | TABLET, FILM COATED | 180 | | 3 |
| 72189-658-90 | Metformin HCL | 90 in 1 BOTTLE | TABLET, FILM COATED | 90 | | 3 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 72189-658-30 | 72189065830 | 30 TABLET, FILM COATED in 1 BOTTLE (72189-658-30) | 2026-01-29 | No | No | Current |
| 72189-658-82 | 72189065882 | 180 TABLET, FILM COATED in 1 BOTTLE (72189-658-82) | 2026-01-29 | No | No | Current |
| 72189-658-90 | 72189065890 | 90 TABLET, FILM COATED in 1 BOTTLE (72189-658-90) | 2026-01-29 | No | No | Current |