Glipizide
- Product NDC
- 21695-469
- 11-digit product format
- 216950469
- Labeler code
- 21695
- Product ID
- 21695-469_e253ec37-78bb-4168-b630-2b7e33607f9d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Glipizide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Rebel Distributors Corp
- Application
- ANDA074223
- Marketing category
- ANDA
- Marketing start
- 1995-02-27
- Marketing end
- 0000-00-00
- Substance
- GLIPIZIDE
- Active strength
- 5 mg/1
- Pharmacologic classes
- Sulfonylurea [EPC],Sulfonylurea Compounds [CS]
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
| Product concept | Relation | Version | Effective |
|---|---|---|---|
| ec4adfb0-aabc-95b9-ad07-5cb8f8533a09 | Product name | 2 | 20250625 |
| b1de1ca9-d9db-4f4b-2103-09e2014d30d5 | Product name | 5 | 20180912 |
| 2dee091b-3b8c-d27a-b1ba-fcb0d32e776a | Product name | 1 | 20140508 |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 21695-469-30 | 2019-09-24 | C162847 | 48780-1 | 934fe258-4983-48b1-e053-8cdaa90a720a | Glipizide Tablets USP Rx only 174347 |
| 21695-469-60 | 2019-09-24 | C162847 | 48780-1 | 934fe258-4983-48b1-e053-8cdaa90a720a | Glipizide Tablets USP Rx only 174347 |
| 21695-469-90 | 2019-09-24 | C162847 | 48780-1 | 934fe258-4983-48b1-e053-8cdaa90a720a | Glipizide Tablets USP Rx only 174347 |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 21695-469-30 | Glipizide | 30 in 1 BOTTLE | TABLET | 30 | 1 | |
| 21695-469-60 | Glipizide | 60 in 1 BOTTLE | TABLET | 60 | 1 | |
| 21695-469-90 | Glipizide | 90 in 1 BOTTLE | TABLET | 90 | 1 |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 21695-469-30 | EA - Each | 21695-469 | f221d6c2-3c2d-47c8-974a-af1dd238965b | 1 | 2012-07-24 |
| 21695-469-60 | EA - Each | 21695-469 | bf8d9b51-8e8e-41ba-b3fd-de70d0ba6ca9 | 1 | 2012-07-24 |
| 21695-469-90 | EA - Each | 21695-469 | f7afe3fa-e97c-4f68-9382-c49f5873aeb7 | 1 | 2012-07-24 |
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|---|---|---|---|---|
| GLIPIZIDE | ACTIVE INGREDIENT | X7WDT95N5C | GLIPIZIDE TABLET [REBEL DISTRIBUTORS CORP] | 1 | |
| GLIPIZIDE | ACTIVE MOIETY | X7WDT95N5C | GLIPIZIDE TABLET [REBEL DISTRIBUTORS CORP] | 1 | |
| ANHYDROUS LACTOSE | INACTIVE INGREDIENT | 3SY5LH9PMK | GLIPIZIDE TABLET [REBEL DISTRIBUTORS CORP] | 1 | |
| CELLULOSE, MICROCRYSTALLINE | INACTIVE INGREDIENT | OP1R32D61U | GLIPIZIDE TABLET [REBEL DISTRIBUTORS CORP] | 1 | |
| COLLOIDAL SILICON DIOXIDE | INACTIVE INGREDIENT | ETJ7Z6XBU4 | GLIPIZIDE TABLET [REBEL DISTRIBUTORS CORP] | 1 | |
| CROSCARMELLOSE SODIUM | INACTIVE INGREDIENT | M28OL1HH48 | GLIPIZIDE TABLET [REBEL DISTRIBUTORS CORP] | 1 | |
| STARCH, CORN | INACTIVE INGREDIENT | O8232NY3SJ | GLIPIZIDE TABLET [REBEL DISTRIBUTORS CORP] | 1 | |
| STEARIC ACID | INACTIVE INGREDIENT | 4ELV7Z65AP | GLIPIZIDE TABLET [REBEL DISTRIBUTORS CORP] | 1 |
DailyMed Dashboard NDC Coverage#
DailyMed RxNorm Mappings#
| RxCUI | RxNorm string | TTY | DailyMed | SPL version |
|---|---|---|---|---|
| 310488 | glipiZIDE 10 MG Oral Tablet | PSN | e253ec37-78bb-4168-b630-2b7e33607f9d | 1 |
| 310490 | glipiZIDE 5 MG Oral Tablet | PSN | e253ec37-78bb-4168-b630-2b7e33607f9d | 1 |
| 310488 | glipizide 10 MG Oral Tablet | SCD | e253ec37-78bb-4168-b630-2b7e33607f9d | 1 |
| 310490 | glipizide 5 MG Oral Tablet | SCD | e253ec37-78bb-4168-b630-2b7e33607f9d | 1 |
Packages#
| Package NDC | 11-digit format | Description | Status |
|---|---|---|---|
| 21695-469-30 | 21695046930 | 30 in 1 BOTTLE | Historical |
| 21695-469-60 | 21695046960 | 60 in 1 BOTTLE | Historical |
| 21695-469-90 | 21695046990 | 90 in 1 BOTTLE | Historical |