Glimepiride
- Product NDC
- 53217-320
- 11-digit product format
- 532170320
- Labeler code
- 53217
- Product ID
- 53217-320_f52b53ee-7651-4329-b137-d546a5e0f986
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Glimepiride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Aidarex Pharmaceuticals LLC
- Application
- ANDA077911
- Marketing category
- ANDA
- Marketing start
- 2012-01-01
- Marketing end
- 0000-00-00
- Substance
- GLIMEPIRIDE
- Active strength
- 4 mg/1
- Pharmacologic classes
- Sulfonylurea [EPC],Sulfonylurea Compounds [CS]
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- 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 |
|---|
| 53217-320-90 | Glimepiride | 90 in 1 BOTTLE | TABLET | 90 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 53217-320 | GLIMEPIRIDE TABLET [AIDAREX PHARMACEUTICALS LLC] | 2 | Legacy NDC, 1 package rows | 20180601_2e1b91a1-f808-4c57-9ef9-743ee4805582.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 53217-320-90 | 53217032090 | 90 in 1 BOTTLE | Historical |