Package 17714-012-10

Brand: acetaminophen

Generic: acetaminophen
NDC Package

Package Facts

Identity

Package NDC 17714-012-10
Digits Only 1771401210
Product NDC 17714-012
Product ID 17714-012_60f41580-e068-faad-e053-2a91aa0a9076
Description

1000 TABLET in 1 BOTTLE (17714-012-10)

Marketing

Marketing Status
Marketed Since 1989-02-05
Brand acetaminophen
Generic acetaminophen
Sample Package No

Linked Drug Pages (1)

Acetaminophen ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "60f41580-e068-faad-e053-2a91aa0a9076", "openfda": {"upc": ["0017714012014"], "unii": ["362O9ITL9D"], "rxcui": ["313782"], "spl_set_id": ["3793a17e-13bf-4d27-b8fa-6753b760f820"], "manufacturer_name": ["Advance Pharmaceutical Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (17714-012-01)", "package_ndc": "17714-012-01", "marketing_start_date": "19890205"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (17714-012-10)", "package_ndc": "17714-012-10", "marketing_start_date": "19890205"}], "brand_name": "Acetaminophen", "product_id": "17714-012_60f41580-e068-faad-e053-2a91aa0a9076", "dosage_form": "TABLET", "product_ndc": "17714-012", "generic_name": "Acetaminophen", "labeler_name": "Advance Pharmaceutical Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Acetaminophen", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "325 mg/1"}], "application_number": "part343", "marketing_category": "OTC MONOGRAPH NOT FINAL", "marketing_start_date": "19890205", "listing_expiration_date": "20261231"}