Package 42192-338-01

Brand: hyoscyamine sulfate odt

Generic: hyoscyamine sulfate
NDC Package

Package Facts

Identity

Package NDC 42192-338-01
Digits Only 4219233801
Product NDC 42192-338
Description

100 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (42192-338-01)

Marketing

Marketing Status
Marketed Since 2011-05-19
Brand hyoscyamine sulfate odt
Generic hyoscyamine sulfate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "41adc6a7-c16a-066d-e063-6394a90affc2", "openfda": {"upc": ["0342192338012"], "unii": ["F2R8V82B84"], "rxcui": ["1046985"], "spl_set_id": ["eef6babc-241f-40b6-b8c8-daa92bbd0a25"], "manufacturer_name": ["Acella Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (42192-338-01)", "package_ndc": "42192-338-01", "marketing_start_date": "20110519"}], "brand_name": "Hyoscyamine Sulfate ODT", "product_id": "42192-338_41adc6a7-c16a-066d-e063-6394a90affc2", "dosage_form": "TABLET, ORALLY DISINTEGRATING", "product_ndc": "42192-338", "generic_name": "hyoscyamine sulfate", "labeler_name": "Acella Pharmaceuticals, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Hyoscyamine Sulfate ODT", "active_ingredients": [{"name": "HYOSCYAMINE SULFATE", "strength": ".125 mg/1"}], "marketing_category": "UNAPPROVED DRUG OTHER", "marketing_start_date": "20110519", "listing_expiration_date": "20261231"}