Allopurinol
- Product NDC
- 53808-0929
- 11-digit product format
- 538080929
- Labeler code
- 53808
- Product ID
- 53808-0929_3da29061-14bf-448a-bf5b-2c4b7f379482
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Allopurinol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- State of Florida DOH Central Pharmacy
- Application
- ANDA090637
- Marketing category
- ANDA
- Marketing start
- 2014-01-01
- Marketing end
- 0000-00-00
- Substance
- ALLOPURINOL
- Active strength
- 100 mg/1
- Pharmacologic classes
- Xanthine Oxidase Inhibitor [EPC],Xanthine Oxidase Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
| Product concept | Relation | Version | Effective |
|---|---|---|---|
| 0ee55bab-4ea8-ac26-c688-380cfbcd5c03 | Product name | 7 | 20260127 |
| de89a493-168f-43fa-9852-1f15e00dbb17 | Product name | 1 | 20221110 |
| 4a2a34d6-1853-423b-9e0c-360370b95802 | Product name | 1 | 20171006 |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 53808-0929-1 | 2020-01-31 | C162847 | 48780-1 | 9d75b9d0-6640-f424-e053-dadaa90a57ce | Allopurinol Tablets, USP 100 mg and 300 mg Rx Only |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 53808-0929-1 | Allopurinol | 30 in 1 BLISTER PACK | TABLET | 30 | 2 |
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|---|---|---|---|---|
| ALLOPURINOL | ACTIVE INGREDIENT | 63CZ7GJN5I | ALLOPURINOL TABLET [STATE OF FLORIDA DOH CENTRAL PHARMACY] | 2 | |
| ALLOPURINOL | ACTIVE MOIETY | 63CZ7GJN5I | ALLOPURINOL TABLET [STATE OF FLORIDA DOH CENTRAL PHARMACY] | 2 | |
| FD&C YELLOW NO. 6 | INACTIVE INGREDIENT | H77VEI93A8 | ALLOPURINOL TABLET [STATE OF FLORIDA DOH CENTRAL PHARMACY] | 2 | |
| LACTOSE MONOHYDRATE | INACTIVE INGREDIENT | EWQ57Q8I5X | ALLOPURINOL TABLET [STATE OF FLORIDA DOH CENTRAL PHARMACY] | 2 | |
| POVIDONE | INACTIVE INGREDIENT | FZ989GH94E | ALLOPURINOL TABLET [STATE OF FLORIDA DOH CENTRAL PHARMACY] | 2 | |
| POVIDONES | INACTIVE INGREDIENT | FZ989GH94E | ALLOPURINOL TABLET [STATE OF FLORIDA DOH CENTRAL PHARMACY] | 2 | |
| SODIUM STARCH GLYCOLATE TYPE A POTATO | INACTIVE INGREDIENT | 5856J3G2A2 | ALLOPURINOL TABLET [STATE OF FLORIDA DOH CENTRAL PHARMACY] | 2 | |
| STARCH, CORN | INACTIVE INGREDIENT | O8232NY3SJ | ALLOPURINOL TABLET [STATE OF FLORIDA DOH CENTRAL PHARMACY] | 2 | |
| STEARIC ACID | INACTIVE INGREDIENT | 4ELV7Z65AP | ALLOPURINOL TABLET [STATE OF FLORIDA DOH CENTRAL PHARMACY] | 2 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 53808-0929 | ALLOPURINOL TABLET [STATE OF FLORIDA DOH CENTRAL PHARMACY] | 2 | Legacy NDC, 1 package rows | 20141219_b9e592ce-942f-4943-a802-bca1c679999f.zip |
DailyMed RxNorm Mappings#
| RxCUI | RxNorm string | TTY | DailyMed | SPL version |
|---|---|---|---|---|
| 197319 | allopurinol 100 MG Oral Tablet | PSN | b9e592ce-942f-4943-a802-bca1c679999f | 2 |
| 197320 | allopurinol 300 MG Oral Tablet | PSN | b9e592ce-942f-4943-a802-bca1c679999f | 2 |
| 197319 | allopurinol 100 MG Oral Tablet | SCD | b9e592ce-942f-4943-a802-bca1c679999f | 2 |
| 197320 | allopurinol 300 MG Oral Tablet | SCD | b9e592ce-942f-4943-a802-bca1c679999f | 2 |
Packages#
| Package NDC | 11-digit format | Description | Status |
|---|---|---|---|
| 53808-0929-1 | 53808092901 | 30 in 1 BLISTER PACK | Historical |