Package 0113-0050-60
Brand: good sense ibuprofen pm
Generic: diphenhydramine citrate, ibuprofenPackage Facts
Identity
Package NDC
0113-0050-60
Digits Only
0113005060
Product NDC
0113-0050
Description
1 BOTTLE in 1 CARTON (0113-0050-60) / 20 TABLET, FILM COATED in 1 BOTTLE
Marketing
Marketing Status
Brand
good sense 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": "c80d2210-786d-4e91-ada6-f89caf3cf6d0", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "unii": ["4OD433S209", "WK2XYI10QM"], "rxcui": ["895664"], "spl_set_id": ["0488786f-9b6b-4935-bb57-bcb2565447f8"], "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": ["L. Perrigo Company"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (0113-0050-58) / 40 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "0113-0050-58", "marketing_start_date": "20090305"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (0113-0050-60) / 20 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "0113-0050-60", "marketing_start_date": "20100507"}], "brand_name": "good sense ibuprofen pm", "product_id": "0113-0050_c80d2210-786d-4e91-ada6-f89caf3cf6d0", "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": "0113-0050", "generic_name": "diphenhydramine citrate, ibuprofen", "labeler_name": "L. Perrigo Company", "product_type": "HUMAN OTC DRUG", "brand_name_base": "good sense 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": "20090305", "listing_expiration_date": "20261231"}