Package 49884-231-83

Brand: praziquantel

Generic: praziquantel
NDC Package

Package Facts

Identity

Package NDC 49884-231-83
Digits Only 4988423183
Product NDC 49884-231
Product ID 49884-231_16be47d2-4bd1-4410-a633-476cdbbbceec
Description

6 TABLET, FILM COATED in 1 BOTTLE (49884-231-83)

Marketing

Marketing Status
Marketed Since 2017-11-27
Brand praziquantel
Generic praziquantel
Sample Package No

Linked Drug Pages (1)

PRAZIQUANTEL ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "16be47d2-4bd1-4410-a633-476cdbbbceec", "openfda": {"nui": ["N0000175481"], "upc": ["0349884231835"], "unii": ["6490C9U457"], "rxcui": ["198140"], "spl_set_id": ["16f2b9c4-a260-4a31-bd52-e5945913246c"], "pharm_class_epc": ["Anthelmintic [EPC]"], "manufacturer_name": ["Endo USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "6 TABLET, FILM COATED in 1 BOTTLE (49884-231-83)", "package_ndc": "49884-231-83", "marketing_start_date": "20171127"}], "brand_name": "PRAZIQUANTEL", "product_id": "49884-231_16be47d2-4bd1-4410-a633-476cdbbbceec", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anthelmintic [EPC]"], "product_ndc": "49884-231", "generic_name": "PRAZIQUANTEL", "labeler_name": "Endo USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "PRAZIQUANTEL", "active_ingredients": [{"name": "PRAZIQUANTEL", "strength": "600 mg/1"}], "application_number": "ANDA208820", "marketing_category": "ANDA", "marketing_start_date": "20171127", "listing_expiration_date": "20261231"}