Allopurinol
- Product NDC
- 69315-409
- 11-digit product format
- 693150409
- Labeler code
- 69315
- Product ID
- 69315-409_227ef709-80a3-45e9-807a-2db8abee3a50
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Allopurinol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Leading Pharma, LLC
- Application
- ANDA214443
- Marketing category
- ANDA
- Marketing start
- 2024-09-01
- Substance
- ALLOPURINOL
- Active strength
- 200 mg/1
- Pharmacologic classes
- Xanthine Oxidase Inhibitor [EPC], Xanthine Oxidase Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Allopurinol
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ALLOPURINOL | 200 mg/1 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 69315-409-09 | Allopurinol | 90 in 1 BOTTLE | TABLET | 90 | | 11 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 69315-409 | ALLOPURINOL TABLET [LEADING PHARMA, LLC] | 11 | Current NDC, 1 package rows | 20240926_f2e8b7fc-936c-585d-e053-2a95a90a1d6c.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 |
|---|
| 69315-409-09 | 69315040909 | 90 TABLET in 1 BOTTLE (69315-409-09) | 90 tablet | 2024-09-01 | No | No | Historical |