allopurinol

Generic: allopurinol

Labeler: mylan institutional inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name allopurinol
Generic Name allopurinol
Labeler mylan institutional inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

allopurinol 100 mg/1

Manufacturer
Mylan Institutional Inc.

Identifiers & Regulatory

Product NDC 51079-205
Product ID 51079-205_3a3943bc-5dca-3650-e063-6394a90afa1b
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA018659
Listing Expiration 2026-12-31
Marketing Start 1997-04-29

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 51079205
Hyphenated Format 51079-205

Supplemental Identifiers

RxCUI
197319 197320
UNII
63CZ7GJN5I
NUI
N0000175698 N0000000206

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 ANDA018659 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 100 mg/1
source: ndc
Packaging
  • 100 BLISTER PACK in 1 CARTON (51079-205-20) / 1 TABLET in 1 BLISTER PACK (51079-205-01)
source: ndc

Packages (1)

51079-205-20 100 BLISTER PACK in 1 CARTON (51079-205-20) / 1 TABLET in 1 BLISTER PACK (51079-205-01)

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": "3a3943bc-5dca-3650-e063-6394a90afa1b", "openfda": {"nui": ["N0000175698", "N0000000206"], "unii": ["63CZ7GJN5I"], "rxcui": ["197319", "197320"], "spl_set_id": ["994b3117-b83e-44d9-910c-1c3a26ef838e"], "pharm_class_epc": ["Xanthine Oxidase Inhibitor [EPC]"], "pharm_class_moa": ["Xanthine Oxidase Inhibitors [MoA]"], "manufacturer_name": ["Mylan Institutional Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 CARTON (51079-205-20)  / 1 TABLET in 1 BLISTER PACK (51079-205-01)", "package_ndc": "51079-205-20", "marketing_start_date": "19970429"}], "brand_name": "Allopurinol", "product_id": "51079-205_3a3943bc-5dca-3650-e063-6394a90afa1b", "dosage_form": "TABLET", "pharm_class": ["Xanthine Oxidase Inhibitor [EPC]", "Xanthine Oxidase Inhibitors [MoA]"], "product_ndc": "51079-205", "generic_name": "allopurinol", "labeler_name": "Mylan Institutional Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Allopurinol", "active_ingredients": [{"name": "ALLOPURINOL", "strength": "100 mg/1"}], "application_number": "ANDA018659", "marketing_category": "ANDA", "marketing_start_date": "19970429", "listing_expiration_date": "20261231"}