Package 55910-050-27

Brand: dg health ibuprofen pm

Generic: diphenhydramine citrate and ibuprofen
NDC Package

Package Facts

Identity

Package NDC 55910-050-27
Digits Only 5591005027
Product NDC 55910-050
Description

1 BOTTLE in 1 CARTON (55910-050-27) / 80 TABLET, FILM COATED in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 2020-03-19
Brand dg health ibuprofen pm
Generic diphenhydramine citrate and ibuprofen
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "6eea1216-fa5d-4c82-a575-e382356d409d", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "unii": ["4OD433S209", "WK2XYI10QM"], "rxcui": ["895664"], "spl_set_id": ["4bbe40de-0957-4705-893d-fcb4191885c9"], "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": ["Dolgencorp Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (55910-050-27)  / 80 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "55910-050-27", "marketing_start_date": "20200319"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (55910-050-60)  / 20 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "55910-050-60", "marketing_start_date": "20100124"}], "brand_name": "dg health Ibuprofen pm", "product_id": "55910-050_6eea1216-fa5d-4c82-a575-e382356d409d", "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": "55910-050", "generic_name": "diphenhydramine citrate and ibuprofen", "labeler_name": "Dolgencorp Inc", "product_type": "HUMAN OTC DRUG", "brand_name_base": "dg health 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": "20100124", "listing_expiration_date": "20261231"}