Glimepiride
- Product NDC
- 0440-6564
- 11-digit product format
- 004406564
- Labeler code
- 0440
- Product ID
- 0440-6564_76103feb-57d5-4cd1-b6fc-ac8825733909
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Glimepiride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Liberty Pharmaceuticals, Inc.
- Application
- ANDA077911
- Marketing category
- ANDA
- Marketing start
- 2012-01-01
- Marketing end
- 0000-00-00
- Substance
- GLIMEPIRIDE
- Active strength
- 1 mg/1
- Pharmacologic classes
- Sulfonylurea [EPC],Sulfonylurea Compounds [CS]
- NDC exclude flag
- E
- Listing certified through
- 2018-12-31
- 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 |
|---|
| 0440-6564-01 | Glimepiride | 100 in 1 BOTTLE | TABLET | 100 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 0440-6564 | GLIMEPIRIDE TABLET [LIBERTY PHARMACEUTICALS, INC.] | 2 | Legacy NDC, 1 package rows | 20160802_c4501673-478e-483e-a7d0-b38fdf75dda2.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 0440-6564-01 | 00440656401 | 100 in 1 BOTTLE | Historical |