Package 17714-013-10

Brand: apap

Generic: acetaminophen
NDC Package

Package Facts

Identity

Package NDC 17714-013-10
Digits Only 1771401310
Product NDC 17714-013
Product ID 17714-013_60f41580-e099-faad-e053-2a91aa0a9076
Description

1000 TABLET in 1 BOTTLE (17714-013-10)

Marketing

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

Linked Drug Pages (1)

APAP ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "60f41580-e099-faad-e053-2a91aa0a9076", "openfda": {"upc": ["0017714013011", "0017714013103"], "unii": ["362O9ITL9D"], "rxcui": ["198440"], "spl_set_id": ["aba26f0a-94e4-4919-a3b0-033e3a9598ef"], "manufacturer_name": ["Advance Pharmaceutical Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (17714-013-01)", "package_ndc": "17714-013-01", "marketing_start_date": "19890205"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (17714-013-10)", "package_ndc": "17714-013-10", "marketing_start_date": "19890205"}], "brand_name": "APAP", "product_id": "17714-013_60f41580-e099-faad-e053-2a91aa0a9076", "dosage_form": "TABLET", "product_ndc": "17714-013", "generic_name": "Acetaminophen", "labeler_name": "Advance Pharmaceutical Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "APAP", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "500 mg/1"}], "application_number": "part343", "marketing_category": "OTC MONOGRAPH NOT FINAL", "marketing_start_date": "19890205", "listing_expiration_date": "20261231"}