allopurinol

Generic: allopurinol

Labeler: florida pharmaceutical products, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name allopurinol
Generic Name allopurinol
Labeler florida pharmaceutical products, llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

allopurinol 100 mg/1

Manufacturer
Florida Pharmaceutical Products, LLC

Identifiers & Regulatory

Product NDC 71921-240
Product ID 71921-240_88cf17e7-9773-490a-992b-63525120cadc
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA204467
Listing Expiration 2027-12-31
Marketing Start 2023-10-31

Pharmacologic Class

Established (EPC)
xanthine oxidase inhibitor [epc]
Mechanism of Action
xanthine oxidase inhibitors [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 71921240
Hyphenated Format 71921-240

Supplemental Identifiers

RxCUI
197319 197320 245422
UPC
0371921240500 0371921240609 0371921242603 0371921242504 0371921241095 0371921240333 0371921242016 0371921240012
UNII
63CZ7GJN5I
NUI
N0000175698 N0000000206

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name allopurinol (source: ndc)
Generic Name allopurinol (source: ndc)
Application Number ANDA204467 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 100 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (71921-240-01)
  • 30 TABLET in 1 BOTTLE (71921-240-33)
  • 500 TABLET in 1 BOTTLE (71921-240-50)
  • 1000 TABLET in 1 BOTTLE (71921-240-60)
source: ndc

Packages (4)

71921-240-01 100 TABLET in 1 BOTTLE (71921-240-01) 71921-240-33 30 TABLET in 1 BOTTLE (71921-240-33) 71921-240-50 500 TABLET in 1 BOTTLE (71921-240-50) 71921-240-60 1000 TABLET in 1 BOTTLE (71921-240-60)

Ingredients (1)

allopurinol (100 mg/1)

Linked Drug Pages (1)

Allopurinol ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "88cf17e7-9773-490a-992b-63525120cadc", "openfda": {"nui": ["N0000175698", "N0000000206"], "upc": ["0371921240500", "0371921240609", "0371921242603", "0371921242504", "0371921241095", "0371921240333", "0371921242016", "0371921240012"], "unii": ["63CZ7GJN5I"], "rxcui": ["197319", "197320", "245422"], "spl_set_id": ["815af471-5985-4819-936d-1f5f3d871ef8"], "pharm_class_epc": ["Xanthine Oxidase Inhibitor [EPC]"], "pharm_class_moa": ["Xanthine Oxidase Inhibitors [MoA]"], "manufacturer_name": ["Florida Pharmaceutical Products, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (71921-240-01)", "package_ndc": "71921-240-01", "marketing_start_date": "20231031"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (71921-240-33)", "package_ndc": "71921-240-33", "marketing_start_date": "20231031"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (71921-240-50)", "package_ndc": "71921-240-50", "marketing_start_date": "20231031"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (71921-240-60)", "package_ndc": "71921-240-60", "marketing_start_date": "20231031"}], "brand_name": "Allopurinol", "product_id": "71921-240_88cf17e7-9773-490a-992b-63525120cadc", "dosage_form": "TABLET", "pharm_class": ["Xanthine Oxidase Inhibitor [EPC]", "Xanthine Oxidase Inhibitors [MoA]"], "product_ndc": "71921-240", "generic_name": "Allopurinol", "labeler_name": "Florida Pharmaceutical Products, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Allopurinol", "active_ingredients": [{"name": "ALLOPURINOL", "strength": "100 mg/1"}], "application_number": "ANDA204467", "marketing_category": "ANDA", "marketing_start_date": "20231031", "listing_expiration_date": "20271231"}