allopurinol

Generic: allopurinol

Labeler: unichem pharmaceuticals (usa), inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name allopurinol
Generic Name allopurinol
Labeler unichem pharmaceuticals (usa), inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

allopurinol 300 mg/1

Manufacturer
Unichem Pharmaceuticals (USA), Inc.

Identifiers & Regulatory

Product NDC 29300-350
Product ID 29300-350_25a9c596-5898-419b-b8bb-c2574fd23d54
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA211820
Listing Expiration 2027-12-31
Marketing Start 2019-03-12

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 29300350
Hyphenated Format 29300-350

Supplemental Identifiers

RxCUI
197319 197320
UPC
0329300350012
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 ANDA211820 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 300 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE, PLASTIC (29300-350-01)
  • 500 TABLET in 1 BOTTLE, PLASTIC (29300-350-05)
  • 1000 TABLET in 1 BOTTLE, PLASTIC (29300-350-10)
source: ndc

Packages (3)

29300-350-01 100 TABLET in 1 BOTTLE, PLASTIC (29300-350-01) 29300-350-05 500 TABLET in 1 BOTTLE, PLASTIC (29300-350-05) 29300-350-10 1000 TABLET in 1 BOTTLE, PLASTIC (29300-350-10)

Ingredients (1)

allopurinol (300 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": "25a9c596-5898-419b-b8bb-c2574fd23d54", "openfda": {"nui": ["N0000175698", "N0000000206"], "upc": ["0329300350012"], "unii": ["63CZ7GJN5I"], "rxcui": ["197319", "197320"], "spl_set_id": ["e3face45-f920-46a0-b707-6a66aa9735bd"], "pharm_class_epc": ["Xanthine Oxidase Inhibitor [EPC]"], "pharm_class_moa": ["Xanthine Oxidase Inhibitors [MoA]"], "manufacturer_name": ["Unichem Pharmaceuticals (USA), Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (29300-350-01)", "package_ndc": "29300-350-01", "marketing_start_date": "20190312"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE, PLASTIC (29300-350-05)", "package_ndc": "29300-350-05", "marketing_start_date": "20190312"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE, PLASTIC (29300-350-10)", "package_ndc": "29300-350-10", "marketing_start_date": "20190312"}], "brand_name": "Allopurinol", "product_id": "29300-350_25a9c596-5898-419b-b8bb-c2574fd23d54", "dosage_form": "TABLET", "pharm_class": ["Xanthine Oxidase Inhibitor [EPC]", "Xanthine Oxidase Inhibitors [MoA]"], "product_ndc": "29300-350", "generic_name": "Allopurinol", "labeler_name": "Unichem Pharmaceuticals (USA), Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Allopurinol", "active_ingredients": [{"name": "ALLOPURINOL", "strength": "300 mg/1"}], "application_number": "ANDA211820", "marketing_category": "ANDA", "marketing_start_date": "20190312", "listing_expiration_date": "20271231"}