Package 51662-1539-1

Brand: ondansetron

Generic: ondansetron
NDC Package

Package Facts

Identity

Package NDC 51662-1539-1
Digits Only 5166215391
Product NDC 51662-1539
Product ID 51662-1539_10351b9f-fb7b-f774-e063-6294a90ad09c
Description

4 BLISTER PACK in 1 BAG (51662-1539-1) / 1 TABLET, FILM COATED in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2021-10-06
Brand ondansetron
Generic ondansetron
Sample Package No

Linked Drug Pages (1)

ONDANSETRON ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "10351b9f-fb7b-f774-e063-6294a90ad09c", "openfda": {"unii": ["NMH84OZK2B"], "rxcui": ["198052"], "spl_set_id": ["cdb2c4b4-a20a-3f8f-e053-2a95a90aaf72"], "manufacturer_name": ["HF Acquisition Co LLC, DBA HealthFirst"]}, "finished": true, "packaging": [{"sample": false, "description": "4 BLISTER PACK in 1 BAG (51662-1539-1)  / 1 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "51662-1539-1", "marketing_start_date": "20211006"}], "brand_name": "ONDANSETRON", "product_id": "51662-1539_10351b9f-fb7b-f774-e063-6294a90ad09c", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin 3 Receptor Antagonists [MoA]", "Serotonin-3 Receptor Antagonist [EPC]"], "product_ndc": "51662-1539", "generic_name": "ONDANSETRON", "labeler_name": "HF Acquisition Co LLC, DBA HealthFirst", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "ONDANSETRON", "active_ingredients": [{"name": "ONDANSETRON HYDROCHLORIDE", "strength": "4 mg/1"}], "application_number": "ANDA076183", "marketing_category": "ANDA", "marketing_start_date": "20211006", "listing_expiration_date": "20261231"}