Package 30142-165-07
Brand: acetaminophen extra strength
Generic: acetaminophenPackage Facts
Identity
Package NDC
30142-165-07
Digits Only
3014216507
Product NDC
30142-165
Description
1 BOTTLE in 1 CARTON (30142-165-07) / 24 TABLET in 1 BOTTLE
Marketing
Marketing Status
Brand
acetaminophen extra strength
Generic
acetaminophen
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "0bd2025f-c8c1-690a-e063-6294a90a439c", "openfda": {"upc": ["0041260012839"], "unii": ["362O9ITL9D"], "rxcui": ["198440"], "spl_set_id": ["b9b6f878-1ec8-3dc0-e053-2995a90a5414"], "manufacturer_name": ["KROGER COMPANY"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (30142-165-07) / 24 TABLET in 1 BOTTLE", "package_ndc": "30142-165-07", "marketing_start_date": "20210306"}], "brand_name": "Acetaminophen Extra Strength", "product_id": "30142-165_0bd2025f-c8c1-690a-e063-6294a90a439c", "dosage_form": "TABLET", "product_ndc": "30142-165", "generic_name": "Acetaminophen", "labeler_name": "KROGER COMPANY", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Acetaminophen Extra Strength", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "500 mg/1"}], "application_number": "M013", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20210306", "listing_expiration_date": "20261231"}