Glipizide
- Product NDC
- 53808-0259
- 11-digit product format
- 538080259
- Labeler code
- 53808
- Product ID
- 53808-0259_120da67b-a619-4a3e-a70a-b7f8bab7a80e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Glipizide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- State of Florida DOH Central Pharmacy
- Application
- ANDA074305
- Marketing category
- ANDA
- Marketing start
- 2009-07-01
- 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
- 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 |
|---|---|---|---|---|---|
| 53808-0259-1 | 2021-01-29 | C162847 | 48780-1 | 956f9ecf-ca26-621f-e053-dbdaa90a74ad | GlipiZIDE Tablets, USP |
| 53808-0259-1 | 2019-10-21 | C162847 | 48780-1 | 956f9ecf-ca26-621f-e053-dbdaa90a74ad | GlipiZIDE Tablets, USP |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 53808-0259-1 | Glipizide | 30 in 1 BLISTER PACK | TABLET | 30 | 2 |
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|---|---|---|---|---|
| GLIPIZIDE | ACTIVE INGREDIENT | X7WDT95N5C | GLIPIZIDE TABLET [STATE OF FLORIDA DOH CENTRAL PHARMACY] | 2 | |
| GLIPIZIDE | ACTIVE MOIETY | X7WDT95N5C | GLIPIZIDE TABLET [STATE OF FLORIDA DOH CENTRAL PHARMACY] | 2 | |
| CELLULOSE, MICROCRYSTALLINE | INACTIVE INGREDIENT | OP1R32D61U | GLIPIZIDE TABLET [STATE OF FLORIDA DOH CENTRAL PHARMACY] | 2 | |
| CROSCARMELLOSE SODIUM | INACTIVE INGREDIENT | M28OL1HH48 | GLIPIZIDE TABLET [STATE OF FLORIDA DOH CENTRAL PHARMACY] | 2 | |
| LACTOSE MONOHYDRATE | INACTIVE INGREDIENT | EWQ57Q8I5X | GLIPIZIDE TABLET [STATE OF FLORIDA DOH CENTRAL PHARMACY] | 2 | |
| MAGNESIUM STEARATE | INACTIVE INGREDIENT | 70097M6I30 | GLIPIZIDE TABLET [STATE OF FLORIDA DOH CENTRAL PHARMACY] | 2 | |
| SILICON DIOXIDE | INACTIVE INGREDIENT | ETJ7Z6XBU4 | GLIPIZIDE TABLET [STATE OF FLORIDA DOH CENTRAL PHARMACY] | 2 | |
| STARCH, CORN | INACTIVE INGREDIENT | O8232NY3SJ | GLIPIZIDE TABLET [STATE OF FLORIDA DOH CENTRAL PHARMACY] | 2 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 53808-0259 | GLIPIZIDE TABLET [STATE OF FLORIDA DOH CENTRAL PHARMACY] | 2 | Legacy NDC, 1 package rows | 20100806_f5b8c777-ec04-44b6-a5c4-251622079aca.zip |
DailyMed RxNorm Mappings#
| RxCUI | RxNorm string | TTY | DailyMed | SPL version |
|---|---|---|---|---|
| 310488 | glipiZIDE 10 MG Oral Tablet | PSN | f5b8c777-ec04-44b6-a5c4-251622079aca | 2 |
| 310490 | glipiZIDE 5 MG Oral Tablet | PSN | f5b8c777-ec04-44b6-a5c4-251622079aca | 2 |
| 310488 | glipizide 10 MG Oral Tablet | SCD | f5b8c777-ec04-44b6-a5c4-251622079aca | 2 |
| 310490 | glipizide 5 MG Oral Tablet | SCD | f5b8c777-ec04-44b6-a5c4-251622079aca | 2 |
Packages#
| Package NDC | 11-digit format | Description | Status |
|---|---|---|---|
| 53808-0259-1 | 53808025901 | 30 in 1 BLISTER PACK | Historical |