Package 68196-919-05

Brand: acetaminophen extra strength

Generic: acetaminophen
NDC Package

Package Facts

Identity

Package NDC 68196-919-05
Digits Only 6819691905
Product NDC 68196-919
Product ID 68196-919_0fc933af-f8b0-46b8-b544-b8b93e40f2d8
Description

400 TABLET, COATED in 1 BOTTLE, PLASTIC (68196-919-05)

Marketing

Marketing Status
Marketed Since 2004-05-10
Brand acetaminophen extra strength
Generic acetaminophen
Sample Package No

Linked Drug Pages (1)

acetaminophen extra strength ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "0fc933af-f8b0-46b8-b544-b8b93e40f2d8", "openfda": {"upc": ["0078742092065"], "unii": ["362O9ITL9D"], "rxcui": ["198440"], "spl_set_id": ["dd99efd0-4ca4-4dc6-a940-bebd17ac8f8d"], "manufacturer_name": ["Sam's West Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "400 TABLET, COATED in 1 BOTTLE, PLASTIC (68196-919-05)", "package_ndc": "68196-919-05", "marketing_start_date": "20040510"}], "brand_name": "acetaminophen extra strength", "product_id": "68196-919_0fc933af-f8b0-46b8-b544-b8b93e40f2d8", "dosage_form": "TABLET, COATED", "product_ndc": "68196-919", "generic_name": "acetaminophen", "labeler_name": "Sam's West Inc", "product_type": "HUMAN OTC DRUG", "brand_name_base": "acetaminophen", "brand_name_suffix": "extra strength", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "500 mg/1"}], "application_number": "M013", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20040510", "listing_expiration_date": "20261231"}