Package 50419-747-01

Brand: biltricide

Generic: praziquantel
NDC Package

Package Facts

Identity

Package NDC 50419-747-01
Digits Only 5041974701
Product NDC 50419-747
Description

6 TABLET, FILM COATED in 1 BOTTLE (50419-747-01)

Marketing

Marketing Status
Marketed Since 2011-04-21
Brand biltricide
Generic praziquantel
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "c9ab40f0-8a11-486f-be88-765af55b6484", "openfda": {"nui": ["N0000175481"], "unii": ["6490C9U457"], "rxcui": ["198140", "208975"], "spl_set_id": ["34ce1cdd-648e-4f1e-8512-bf3d4cc22eb9"], "pharm_class_epc": ["Anthelmintic [EPC]"], "manufacturer_name": ["Bayer HealthCare Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "6 TABLET, FILM COATED in 1 BOTTLE (50419-747-01)", "package_ndc": "50419-747-01", "marketing_start_date": "20110421"}], "brand_name": "Biltricide", "product_id": "50419-747_c9ab40f0-8a11-486f-be88-765af55b6484", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anthelmintic [EPC]"], "product_ndc": "50419-747", "generic_name": "praziquantel", "labeler_name": "Bayer HealthCare Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Biltricide", "active_ingredients": [{"name": "PRAZIQUANTEL", "strength": "600 mg/1"}], "application_number": "NDA018714", "marketing_category": "NDA", "marketing_start_date": "20110421", "listing_expiration_date": "20271231"}