Package 66715-6417-8
Brand: tylenol pm extra strength, cvp health
Generic: acetaminophen and diphenhydramine hydrochloridePackage Facts
Identity
Package NDC
66715-6417-8
Digits Only
6671564178
Product NDC
66715-6417
Description
30 POUCH in 1 CARTON (66715-6417-8) / 2 TABLET, FILM COATED in 1 POUCH
Marketing
Marketing Status
Brand
tylenol pm extra strength, cvp health
Generic
acetaminophen and diphenhydramine hydrochloride
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "459f9062-e920-d327-e063-6394a90acc1d", "openfda": {"unii": ["362O9ITL9D", "TC2D6JAD40"], "rxcui": ["1092189", "1092378"], "spl_set_id": ["643371f2-e330-441e-8932-b3aec4b179d2"], "manufacturer_name": ["Lil' Drug Store Products, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "2 POUCH in 1 CARTON (66715-6417-2) / 2 TABLET, FILM COATED in 1 POUCH", "package_ndc": "66715-6417-2", "marketing_start_date": "20221011"}, {"sample": false, "description": "25 POUCH in 1 CARTON (66715-6417-7) / 2 TABLET, FILM COATED in 1 POUCH", "package_ndc": "66715-6417-7", "marketing_end_date": "20280812", "marketing_start_date": "20220419"}, {"sample": false, "description": "30 POUCH in 1 CARTON (66715-6417-8) / 2 TABLET, FILM COATED in 1 POUCH", "package_ndc": "66715-6417-8", "marketing_start_date": "20220419"}], "brand_name": "Tylenol PM Extra Strength, CVP HEALTH", "product_id": "66715-6417_459f9062-e920-d327-e063-6394a90acc1d", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "66715-6417", "generic_name": "Acetaminophen and Diphenhydramine Hydrochloride", "labeler_name": "Lil' Drug Store Products, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Tylenol PM Extra Strength, CVP HEALTH", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "500 mg/1"}, {"name": "DIPHENHYDRAMINE HYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "M013", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20220419", "listing_expiration_date": "20261231"}