Package 65862-187-30

Brand: ondansetron hydrochloride

Generic: ondansetron hydrochloride
NDC Package

Package Facts

Identity

Package NDC 65862-187-30
Digits Only 6586218730
Product NDC 65862-187
Product ID 65862-187_8934ad79-3eda-46d1-b527-53d122760a89
Description

30 TABLET, FILM COATED in 1 BOTTLE (65862-187-30)

Marketing

Marketing Status
Marketed Since 2007-07-31
Brand ondansetron hydrochloride
Generic ondansetron hydrochloride
Sample Package No

Linked Drug Pages (1)

Ondansetron Hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "8934ad79-3eda-46d1-b527-53d122760a89", "openfda": {"unii": ["NMH84OZK2B"], "rxcui": ["198052", "312084", "312086"], "spl_set_id": ["57578387-1918-4e56-a564-f14fb22340bf"], "manufacturer_name": ["Aurobindo Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BLISTER PACK in 1 CARTON (65862-187-03)  / 3 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "65862-187-03", "marketing_start_date": "20070731"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (65862-187-05)", "package_ndc": "65862-187-05", "marketing_start_date": "20070731"}, {"sample": false, "description": "10 BLISTER PACK in 1 CARTON (65862-187-10)  / 10 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "65862-187-10", "marketing_start_date": "20070731"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (65862-187-30)", "package_ndc": "65862-187-30", "marketing_start_date": "20070731"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (65862-187-99)", "package_ndc": "65862-187-99", "marketing_start_date": "20070731"}], "brand_name": "Ondansetron Hydrochloride", "product_id": "65862-187_8934ad79-3eda-46d1-b527-53d122760a89", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin 3 Receptor Antagonists [MoA]", "Serotonin-3 Receptor Antagonist [EPC]"], "product_ndc": "65862-187", "generic_name": "Ondansetron Hydrochloride", "labeler_name": "Aurobindo Pharma Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ondansetron Hydrochloride", "active_ingredients": [{"name": "ONDANSETRON HYDROCHLORIDE", "strength": "4 mg/1"}], "application_number": "ANDA078539", "marketing_category": "ANDA", "marketing_start_date": "20070731", "listing_expiration_date": "20261231"}