Package 71930-010-30

Brand: alosetron hydrochloride

Generic: alosetron hydrochloride
NDC Package

Package Facts

Identity

Package NDC 71930-010-30
Digits Only 7193001030
Product NDC 71930-010
Description

30 TABLET in 1 BOTTLE (71930-010-30)

Marketing

Marketing Status
Marketed Since 2019-02-01
Brand alosetron hydrochloride
Generic alosetron hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "c304be8d-9fa3-4d89-885e-5a6bf1e80a2b", "openfda": {"upc": ["0371930010309", "0371930011306"], "unii": ["2F5R1A46YW"], "rxcui": ["259306", "403975"], "spl_set_id": ["d62b2c5a-1693-4e67-96d5-197e1fdc8694"], "manufacturer_name": ["Eywa Pharma Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (71930-010-30)", "package_ndc": "71930-010-30", "marketing_start_date": "20190201"}], "brand_name": "Alosetron Hydrochloride", "product_id": "71930-010_c304be8d-9fa3-4d89-885e-5a6bf1e80a2b", "dosage_form": "TABLET", "pharm_class": ["Serotonin 3 Receptor Antagonists [MoA]", "Serotonin-3 Receptor Antagonist [EPC]"], "product_ndc": "71930-010", "generic_name": "Alosetron Hydrochloride", "labeler_name": "Eywa Pharma Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Alosetron Hydrochloride", "active_ingredients": [{"name": "ALOSETRON HYDROCHLORIDE", "strength": ".5 mg/1"}], "application_number": "ANDA211621", "marketing_category": "ANDA", "marketing_start_date": "20190201", "listing_expiration_date": "20261231"}