Package 65862-782-01

Brand: methenamine hippurate

Generic: methenamine hippurate
NDC Package

Package Facts

Identity

Package NDC 65862-782-01
Digits Only 6586278201
Product NDC 65862-782
Product ID 65862-782_f28fb98d-95dd-4beb-9bd8-1c066233c86f
Description

100 TABLET in 1 BOTTLE (65862-782-01)

Marketing

Marketing Status
Marketed Since 2016-07-05
Brand methenamine hippurate
Generic methenamine hippurate
Sample Package No

Linked Drug Pages (1)

Methenamine Hippurate ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "f28fb98d-95dd-4beb-9bd8-1c066233c86f", "openfda": {"unii": ["M329791L57"], "rxcui": ["992150"], "spl_set_id": ["9f002ad9-58e7-44f2-a980-3cc3f36bbd9b"], "manufacturer_name": ["Aurobindo Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (65862-782-01)", "package_ndc": "65862-782-01", "marketing_start_date": "20160705"}], "brand_name": "Methenamine Hippurate", "product_id": "65862-782_f28fb98d-95dd-4beb-9bd8-1c066233c86f", "dosage_form": "TABLET", "product_ndc": "65862-782", "generic_name": "Methenamine Hippurate", "labeler_name": "Aurobindo Pharma Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Methenamine Hippurate", "active_ingredients": [{"name": "METHENAMINE HIPPURATE", "strength": "1 g/1"}], "application_number": "ANDA205661", "marketing_category": "ANDA", "marketing_start_date": "20160705", "listing_expiration_date": "20261231"}