Allopurinol
- Product NDC
- 51655-523
- 11-digit product format
- 516550523
- Labeler code
- 51655
- Product ID
- 51655-523_494dda25-b095-7fc2-e063-6394a90a8a36
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- allopurinol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Northwind Health Company, LLC
- Application
- ANDA203154
- Marketing category
- ANDA
- Marketing start
- 2022-09-06
- Substance
- ALLOPURINOL
- Active strength
- 100 mg/1
- Pharmacologic classes
- Xanthine Oxidase Inhibitor [EPC], Xanthine Oxidase Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Allopurinol
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ALLOPURINOL | 100 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 63CZ7GJN5I |
| Rxcui | 197319 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 51655-523-52 | Allopurinol | 30 in 1 BOTTLE, PLASTIC | TABLET | 30 | | 14 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 51655-523 | ALLOPURINOL TABLET [NORTHWIND PHARMACEUTICALS, LLC] | 13 | Current NDC, 1 package rows | 20241225_f3198e1b-6344-ad96-e053-2995a90a4aaf.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 51655-523-52 | 51655052352 | 30 TABLET in 1 BOTTLE, PLASTIC (51655-523-52) | 30 tablet | 2022-09-06 | No | No | Historical |