Glimepiride
- Product NDC
- 43063-699
- 11-digit product format
- 430630699
- Labeler code
- 43063
- Product ID
- 43063-699_4d61d305-dfb6-c3a2-e063-6394a90a4a73
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Glimepiride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Application
- ANDA077911
- Marketing category
- ANDA
- Marketing start
- 2012-01-01
- Substance
- GLIMEPIRIDE
- Active strength
- 4 mg/1
- Pharmacologic classes
- Sulfonylurea Compounds [CS], Sulfonylurea [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Glimepiride
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| GLIMEPIRIDE | 4 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 6KY687524K |
| Rxcui | 199247 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 43063-699-90 | Glimepiride | 90 in 1 BOTTLE, PLASTIC | TABLET | 90 | | 21 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 43063-699 | GLIMEPIRIDE TABLET [PD-RX PHARMACEUTICALS, INC.] | 20 | Current NDC, Legacy NDC, 1 package rows | 20250112_647a146c-c752-4589-8619-aed5c720ca54.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 |
|---|
| 43063-699-90 | 43063069990 | 90 TABLET in 1 BOTTLE, PLASTIC (43063-699-90) | 90 tablet | 2016-08-01 | 0000-00-00 | No | No | Current |
| 43063-699-93 | 43063069993 | 180 TABLET in 1 BOTTLE, PLASTIC (43063-699-93) | 180 tablet | 2016-08-01 | 0000-00-00 | No | No | Current |