allopurinol

Generic: allopurinol

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

Drug Facts

Product Profile

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

allopurinol 300 mg/1

Manufacturer
REMEDYREPACK INC.

Identifiers & Regulatory

Product NDC 70518-3704
Product ID 70518-3704_4c1ff040-a553-5f0f-e063-6294a90ab94c
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA211820
Listing Expiration 2027-12-31
Marketing Start 2023-04-07

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 705183704
Hyphenated Format 70518-3704

Supplemental Identifiers

RxCUI
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 ANDA211820 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 300 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BLISTER PACK (70518-3704-0)
  • 100 TABLET in 1 BOTTLE, PLASTIC (70518-3704-1)
  • 90 TABLET in 1 BOTTLE, PLASTIC (70518-3704-3)
source: ndc

Packages (3)

70518-3704-0 30 TABLET in 1 BLISTER PACK (70518-3704-0) 70518-3704-1 100 TABLET in 1 BOTTLE, PLASTIC (70518-3704-1) 70518-3704-3 90 TABLET in 1 BOTTLE, PLASTIC (70518-3704-3)

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": "4c1ff040-a553-5f0f-e063-6294a90ab94c", "openfda": {"nui": ["N0000175698", "N0000000206"], "unii": ["63CZ7GJN5I"], "rxcui": ["197320"], "spl_set_id": ["5ffcbc32-5996-41cd-acdc-cc4af8cdaf4f"], "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 (70518-3704-0)", "package_ndc": "70518-3704-0", "marketing_start_date": "20230407"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (70518-3704-1)", "package_ndc": "70518-3704-1", "marketing_start_date": "20240201"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (70518-3704-3)", "package_ndc": "70518-3704-3", "marketing_start_date": "20250721"}], "brand_name": "Allopurinol", "product_id": "70518-3704_4c1ff040-a553-5f0f-e063-6294a90ab94c", "dosage_form": "TABLET", "pharm_class": ["Xanthine Oxidase Inhibitor [EPC]", "Xanthine Oxidase Inhibitors [MoA]"], "product_ndc": "70518-3704", "generic_name": "Allopurinol", "labeler_name": "REMEDYREPACK 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": "20230407", "listing_expiration_date": "20271231"}