Allopurinol

Generic: allopurinol

Labeler: REMEDYREPACK INC.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Active

Drug Facts

Product Profile

Brand Name Allopurinol
Generic Name allopurinol
Labeler REMEDYREPACK INC.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

ALLOPURINOL 100 mg/1

Identifiers & Regulatory

Product NDC 70518-0476
Product ID 70518-0476_47f7337b-b613-9bb5-e063-6294a90a09b2
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA075798
Listing Expiration 2027-12-31
Marketing Start 2017-05-12

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 705180476
Hyphenated Format 70518-0476

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 ANDA075798 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 100 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BLISTER PACK (70518-0476-1)
source: ndc

Packages (1)

70518-0476-1 30 TABLET in 1 BLISTER PACK (70518-0476-1)

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": "47f7337b-b613-9bb5-e063-6294a90a09b2", "openfda": {"nui": ["N0000175698", "N0000000206"], "unii": ["63CZ7GJN5I"], "rxcui": ["197319"], "spl_set_id": ["9138122e-844c-4613-b70e-e60d5ffcbd13"], "pharm_class_epc": ["Xanthine Oxidase Inhibitor [EPC]"], "pharm_class_moa": ["Xanthine Oxidase Inhibitors [MoA]"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BLISTER PACK (70518-0476-1)", "package_ndc": "70518-0476-1", "marketing_start_date": "20250210"}], "brand_name": "Allopurinol", "product_id": "70518-0476_47f7337b-b613-9bb5-e063-6294a90a09b2", "dosage_form": "TABLET", "pharm_class": ["Xanthine Oxidase Inhibitor [EPC]", "Xanthine Oxidase Inhibitors [MoA]"], "product_ndc": "70518-0476", "generic_name": "allopurinol", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Allopurinol", "active_ingredients": [{"name": "ALLOPURINOL", "strength": "100 mg/1"}], "application_number": "ANDA075798", "marketing_category": "ANDA", "marketing_start_date": "20170512", "listing_expiration_date": "20271231"}