Glipizide and metformin hcl
- Product NDC
- 62135-731
- 11-digit product format
- 621350731
- Labeler code
- 62135
- Product ID
- 62135-731_459bebab-b18b-58b4-e063-6294a90ad140
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Glipizide and metformin hcl
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Chartwell RX, LLC
- Application
- ANDA078728
- Marketing category
- ANDA
- Marketing start
- 2010-06-29
- Substance
- GLIPIZIDE; METFORMIN HYDROCHLORIDE
- Active strength
- 2.5; 250 mg/1; mg/1
- Pharmacologic classes
- Biguanide [EPC], Biguanides [CS], Sulfonylurea Compounds [CS], Sulfonylurea [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Glipizide and metformin hcl
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| GLIPIZIDE | 2.5 mg/1 |
| METFORMIN HYDROCHLORIDE | 250 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | X7WDT95N5C, 786Z46389E |
| Rxcui | 861731, 861736, 861740 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 62135-731-60 | Glipizide and metformin hcl | 60 in 1 BOTTLE | TABLET, FILM COATED | 60 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 62135-731 | GLIPIZIDE AND METFORMIN HCL TABLET, FILM COATED [CHARTWELL RX, LLC] | 2 | Current NDC, 1 package rows | 20241030_ac018f64-fd9d-4b3c-b0ac-ca305b8df635.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 62135-731-60 | 62135073160 | 60 TABLET, FILM COATED in 1 BOTTLE (62135-731-60) | 2023-08-15 | No | No | Historical |