Package 68016-303-01

Brand: arthritis pain relief

Generic: acetaminophen
NDC Package

Package Facts

Identity

Package NDC 68016-303-01
Digits Only 6801630301
Product NDC 68016-303
Product ID 68016-303_243426e7-9529-c46a-e063-6394a90a9341
Description

100 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (68016-303-01)

Marketing

Marketing Status
Discontinued 2026-09-30
Brand arthritis pain relief
Generic acetaminophen
Sample Package No

Linked Drug Pages (1)

Arthritis Pain Relief ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "243426e7-9529-c46a-e063-6394a90a9341", "openfda": {"upc": ["0840986036897"], "unii": ["362O9ITL9D"], "rxcui": ["1148399"], "spl_set_id": ["778a15d5-3fa4-4386-8afb-751f4537c10d"], "manufacturer_name": ["CHAIN DRUG CONSORTIUM"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (68016-303-01)", "package_ndc": "68016-303-01", "marketing_end_date": "20260930", "marketing_start_date": "20200801"}, {"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (68016-303-50)  / 50 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC", "package_ndc": "68016-303-50", "marketing_end_date": "20260630", "marketing_start_date": "20200801"}], "brand_name": "Arthritis Pain Relief", "product_id": "68016-303_243426e7-9529-c46a-e063-6394a90a9341", "dosage_form": "TABLET, EXTENDED RELEASE", "product_ndc": "68016-303", "generic_name": "Acetaminophen", "labeler_name": "CHAIN DRUG CONSORTIUM", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Arthritis Pain Relief", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "650 mg/1"}], "application_number": "ANDA211544", "marketing_category": "ANDA", "marketing_end_date": "20260930", "marketing_start_date": "20200801"}