Package 41250-050-58

Brand: ibuprofen pm

Generic: diphenhydramine citrate, ibuprofen
NDC Package

Package Facts

Identity

Package NDC 41250-050-58
Digits Only 4125005058
Product NDC 41250-050
Description

1 BOTTLE in 1 CARTON (41250-050-58) / 40 TABLET, FILM COATED in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 2009-04-08
Brand ibuprofen pm
Generic diphenhydramine citrate, ibuprofen
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "0b78b2f5-ea42-4f46-9756-9be8a6d0d467", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "unii": ["4OD433S209", "WK2XYI10QM"], "rxcui": ["895664"], "spl_set_id": ["47e71e23-da8a-4759-ac5a-1d48e0d9ab98"], "pharm_class_cs": ["Anti-Inflammatory Agents, Non-Steroidal [CS]"], "pharm_class_epc": ["Nonsteroidal Anti-inflammatory Drug [EPC]"], "pharm_class_moa": ["Cyclooxygenase Inhibitors [MoA]"], "manufacturer_name": ["Meijer Distribution Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (41250-050-58)  / 40 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "41250-050-58", "marketing_start_date": "20090408"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (41250-050-76)  / 120 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "41250-050-76", "marketing_start_date": "20171021"}], "brand_name": "Ibuprofen PM", "product_id": "41250-050_0b78b2f5-ea42-4f46-9756-9be8a6d0d467", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "41250-050", "generic_name": "diphenhydramine citrate, ibuprofen", "labeler_name": "Meijer Distribution Inc", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Ibuprofen PM", "active_ingredients": [{"name": "DIPHENHYDRAMINE CITRATE", "strength": "38 mg/1"}, {"name": "IBUPROFEN", "strength": "200 mg/1"}], "application_number": "ANDA079113", "marketing_category": "ANDA", "marketing_start_date": "20090408", "listing_expiration_date": "20261231"}