Package 49035-699-60

Brand: equate ibuprofen pm

Generic: diphenhydramine citrate, ibuprofen
NDC Package

Package Facts

Identity

Package NDC 49035-699-60
Digits Only 4903569960
Product NDC 49035-699
Description

1 BOTTLE in 1 CARTON (49035-699-60) / 20 TABLET, FILM COATED in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 2009-04-15
Brand equate 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": "d2f10efb-2d93-4050-83b6-ff227b5ef1da", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "unii": ["4OD433S209", "WK2XYI10QM"], "rxcui": ["895664"], "spl_set_id": ["e36957ed-653c-465f-8150-7d6073e1376f"], "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": ["Wal-Mart Stores Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (49035-699-27)  / 80 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "49035-699-27", "marketing_start_date": "20090415"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (49035-699-60)  / 20 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "49035-699-60", "marketing_start_date": "20090415"}], "brand_name": "equate ibuprofen pm", "product_id": "49035-699_d2f10efb-2d93-4050-83b6-ff227b5ef1da", "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": "49035-699", "generic_name": "diphenhydramine citrate, ibuprofen", "labeler_name": "Wal-Mart Stores Inc", "product_type": "HUMAN OTC DRUG", "brand_name_base": "equate 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": "20090415", "listing_expiration_date": "20261231"}