Package 0363-2035-08
Brand: pain reliever pm
Generic: acetaminophen, diphenhydramine hclPackage Facts
Identity
Package NDC
0363-2035-08
Digits Only
0363203508
Product NDC
0363-2035
Description
1 BOTTLE, PLASTIC in 1 CARTON (0363-2035-08) / 24 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
Marketing
Marketing Status
Brand
pain reliever pm
Generic
acetaminophen, diphenhydramine hcl
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "7aaebcc7-8d29-4f7d-b737-224bcf940f53", "openfda": {"upc": ["0311917160351"], "unii": ["362O9ITL9D", "TC2D6JAD40"], "rxcui": ["1092189"], "spl_set_id": ["9655c38a-126b-459e-b31d-0aa33d9eb522"], "manufacturer_name": ["Walgreen Company"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (0363-2035-08) / 24 TABLET, FILM COATED in 1 BOTTLE, PLASTIC", "package_ndc": "0363-2035-08", "marketing_start_date": "19940515"}], "brand_name": "Pain Reliever PM", "product_id": "0363-2035_7aaebcc7-8d29-4f7d-b737-224bcf940f53", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "0363-2035", "generic_name": "Acetaminophen, Diphenhydramine HCl", "labeler_name": "Walgreen Company", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Pain Reliever PM", "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": "19940515", "listing_expiration_date": "20261231"}