Glipizide
- Product NDC
- 52959-822
- 11-digit product format
- 529590822
- Labeler code
- 52959
- Product ID
- 52959-822_ad2e35e9-f17a-4a7a-a19d-bfe7af334161
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Glipizide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- H.J. Harkins Company, Inc.
- Application
- ANDA074223
- Marketing category
- ANDA
- Marketing start
- 1995-02-27
- Marketing end
- 0000-00-00
- Substance
- GLIPIZIDE
- Active strength
- 10 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 |
|---|
| 52959-822-00 | Glipizide | 100 in 1 BOTTLE, PLASTIC | TABLET | 100 | | 1 |
| 52959-822-30 | Glipizide | 30 in 1 BOTTLE, PLASTIC | TABLET | 30 | | 1 |
| 52959-822-60 | Glipizide | 60 in 1 BOTTLE, PLASTIC | TABLET | 60 | | 1 |
DailyMed Socrata Ingredients#
Ingredient, Type, UNII table| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|
| GLIPIZIDE | ACTIVE INGREDIENT | X7WDT95N5C | GLIPIZIDE TABLET [H.J. HARKINS COMPANY, INC.] | 1 | |
| GLIPIZIDE | ACTIVE MOIETY | X7WDT95N5C | GLIPIZIDE TABLET [H.J. HARKINS COMPANY, INC.] | 1 | |
| ANHYDROUS LACTOSE | INACTIVE INGREDIENT | 3SY5LH9PMK | GLIPIZIDE TABLET [H.J. HARKINS COMPANY, INC.] | 1 | |
| CELLULOSE, MICROCRYSTALLINE | INACTIVE INGREDIENT | OP1R32D61U | GLIPIZIDE TABLET [H.J. HARKINS COMPANY, INC.] | 1 | |
| COLLOIDAL SILICON DIOXIDE | INACTIVE INGREDIENT | ETJ7Z6XBU4 | GLIPIZIDE TABLET [H.J. HARKINS COMPANY, INC.] | 1 | |
| CROSCARMELLOSE SODIUM | INACTIVE INGREDIENT | M28OL1HH48 | GLIPIZIDE TABLET [H.J. HARKINS COMPANY, INC.] | 1 | |
| STARCH, CORN | INACTIVE INGREDIENT | O8232NY3SJ | GLIPIZIDE TABLET [H.J. HARKINS COMPANY, INC.] | 1 | |
| STEARIC ACID | INACTIVE INGREDIENT | 4ELV7Z65AP | GLIPIZIDE TABLET [H.J. HARKINS COMPANY, INC.] | 1 | |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 52959-822 | GLIPIZIDE TABLET [H.J. HARKINS COMPANY, INC.] | 1 | Legacy NDC, 3 package rows | 20111208_0a280a88-5973-4d0f-9b25-9be0c96e49c7.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 52959-822-00 | 52959082200 | 100 in 1 BOTTLE, PLASTIC | Historical |
| 52959-822-30 | 52959082230 | 30 in 1 BOTTLE, PLASTIC | Historical |
| 52959-822-60 | 52959082260 | 60 in 1 BOTTLE, PLASTIC | Historical |