Package 49502-476-26

Brand: pretomanid

Generic: pretomanid
NDC Package

Package Facts

Identity

Package NDC 49502-476-26
Digits Only 4950247626
Product NDC 49502-476
Description

1 BOTTLE in 1 CARTON (49502-476-26) / 26 TABLET in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 2019-11-07
Brand pretomanid
Generic pretomanid
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "99ba96bb-da73-4082-bb81-c573f6019013", "openfda": {"nui": ["N0000175483", "N0000190111"], "unii": ["2XOI31YC4N"], "rxcui": ["2198370"], "spl_set_id": ["f1906fc9-cb3c-4e13-8a4a-da76100c1bf3"], "pharm_class_epc": ["Antimycobacterial [EPC]"], "pharm_class_moa": ["Organic Anion Transporter 3 Inhibitors [MoA]"], "manufacturer_name": ["Viatris Specialty LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (49502-476-26)  / 26 TABLET in 1 BOTTLE", "package_ndc": "49502-476-26", "marketing_start_date": "20191107"}], "brand_name": "Pretomanid", "product_id": "49502-476_99ba96bb-da73-4082-bb81-c573f6019013", "dosage_form": "TABLET", "pharm_class": ["Antimycobacterial [EPC]", "Organic Anion Transporter 3 Inhibitors [MoA]"], "product_ndc": "49502-476", "generic_name": "Pretomanid", "labeler_name": "Viatris Specialty LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Pretomanid", "active_ingredients": [{"name": "PRETOMANID", "strength": "200 mg/1"}], "application_number": "NDA212862", "marketing_category": "NDA", "marketing_start_date": "20191107", "listing_expiration_date": "20261231"}