Package 79481-0149-1
Brand: meijer extra strength pain relief pm caplet
Generic: acetaminophen, diphenhydramine hydrochloridePackage Facts
Identity
Package NDC
79481-0149-1
Digits Only
7948101491
Product NDC
79481-0149
Description
1 BOTTLE in 1 CARTON (79481-0149-1) / 100 TABLET in 1 BOTTLE
Marketing
Marketing Status
Brand
meijer extra strength pain relief pm caplet
Generic
acetaminophen, diphenhydramine hydrochloride
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "01e1af5f-2c74-4f27-9273-7470656e21f7", "openfda": {"upc": ["0713733981262"], "unii": ["362O9ITL9D", "TC2D6JAD40"], "rxcui": ["1092189"], "spl_set_id": ["1bee7e4f-1813-1bdf-e063-6294a90a6a32"], "manufacturer_name": ["Meijer, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (79481-0149-1) / 100 TABLET in 1 BOTTLE", "package_ndc": "79481-0149-1", "marketing_start_date": "20240627"}, {"sample": false, "description": "2 BOTTLE in 1 CARTON (79481-0149-2) / 100 TABLET in 1 BOTTLE", "package_ndc": "79481-0149-2", "marketing_start_date": "20240627"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (79481-0149-3) / 24 TABLET in 1 BOTTLE", "package_ndc": "79481-0149-3", "marketing_start_date": "20250217"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (79481-0149-5) / 50 TABLET in 1 BOTTLE", "package_ndc": "79481-0149-5", "marketing_start_date": "20240627"}], "brand_name": "meijer EXTRA STRENGTH Pain Relief PM Caplet", "product_id": "79481-0149_01e1af5f-2c74-4f27-9273-7470656e21f7", "dosage_form": "TABLET", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "79481-0149", "generic_name": "Acetaminophen, Diphenhydramine hydrochloride", "labeler_name": "Meijer, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "meijer EXTRA STRENGTH Pain Relief PM Caplet", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "500 mg/1"}, {"name": "DIPHENHYDRAMINE HYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20240627", "listing_expiration_date": "20261231"}