Glyburide
- Product NDC
- 33261-209
- 11-digit product format
- 332610209
- Labeler code
- 33261
- Product ID
- 33261-209_fea6f761-235f-4d3d-99c6-6389070ec7d9
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Glyburide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Aidarex Pharmaceuticals LLC
- Application
- ANDA090937
- Marketing category
- ANDA
- Marketing start
- 2010-10-05
- Marketing end
- 0000-00-00
- Substance
- GLYBURIDE
- Active strength
- 5 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 |
|---|
| 33261-209-30 | Glyburide | 30 in 1 BOTTLE, PLASTIC | TABLET | 30 | | 1 |
| 33261-209-60 | Glyburide | 60 in 1 BOTTLE, PLASTIC | TABLET | 60 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 33261-209 | GLYBURIDE TABLET [AIDAREX PHARMACEUTICALS LLC] | 1 | Legacy NDC, 2 package rows | 20140110_04201349-2a01-4fc1-9920-1ef7376d352f.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 33261-209-30 | 33261020930 | 30 in 1 BOTTLE, PLASTIC | Historical |
| 33261-209-60 | 33261020960 | 60 in 1 BOTTLE, PLASTIC | Historical |