allopurinol
Generic: allopurinol
Labeler: indoco remedies limitedDrug Facts
Product Profile
Brand Name
allopurinol
Generic Name
allopurinol
Labeler
indoco remedies limited
Dosage Form
TABLET
Routes
Active Ingredients
allopurinol 100 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
14445-170
Product ID
14445-170_7394738d-e6ca-4be9-9fb8-28702362abc5
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA204467
Listing Expiration
2026-12-31
Marketing Start
2016-07-28
Pharmacologic Class
Established (EPC)
Mechanism of Action
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
14445170
Hyphenated Format
14445-170
Supplemental Identifiers
RxCUI
UPC
UNII
NUI
Packaging Origin
Original Packager
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
source: ndc
Resolved Composition
Strengths
- 100 mg/1
Packaging
- 1000 TABLET in 1 BOTTLE (14445-170-00)
- 100 TABLET in 1 BOTTLE (14445-170-01)
- 500 TABLET in 1 BOTTLE (14445-170-05)
- 30 TABLET in 1 BOTTLE (14445-170-30)
Packages (4)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "7394738d-e6ca-4be9-9fb8-28702362abc5", "openfda": {"nui": ["N0000175698", "N0000000206"], "upc": ["0314445172100"], "unii": ["63CZ7GJN5I"], "rxcui": ["197319", "197320", "245422"], "spl_set_id": ["48a9a6c3-4604-421e-a323-1133888aaf76"], "pharm_class_epc": ["Xanthine Oxidase Inhibitor [EPC]"], "pharm_class_moa": ["Xanthine Oxidase Inhibitors [MoA]"], "manufacturer_name": ["Indoco Remedies Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET in 1 BOTTLE (14445-170-00)", "package_ndc": "14445-170-00", "marketing_start_date": "20160728"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (14445-170-01)", "package_ndc": "14445-170-01", "marketing_start_date": "20160728"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (14445-170-05)", "package_ndc": "14445-170-05", "marketing_start_date": "20160728"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (14445-170-30)", "package_ndc": "14445-170-30", "marketing_start_date": "20160728"}], "brand_name": "Allopurinol", "product_id": "14445-170_7394738d-e6ca-4be9-9fb8-28702362abc5", "dosage_form": "TABLET", "pharm_class": ["Xanthine Oxidase Inhibitor [EPC]", "Xanthine Oxidase Inhibitors [MoA]"], "product_ndc": "14445-170", "generic_name": "Allopurinol", "labeler_name": "Indoco Remedies Limited", "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": "20160728", "listing_expiration_date": "20261231"}