Package 70756-702-30

Brand: alosetron

Generic: alosetron
NDC Package

Package Facts

Identity

Package NDC 70756-702-30
Digits Only 7075670230
Product NDC 70756-702
Product ID 70756-702_6e1e5a99-5018-42e7-8e2c-bcd0ac1e80fb
Description

30 TABLET in 1 BOTTLE (70756-702-30)

Marketing

Marketing Status
Marketed Since 2020-09-14
Brand alosetron
Generic alosetron
Sample Package No

Linked Drug Pages (1)

Alosetron ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "6e1e5a99-5018-42e7-8e2c-bcd0ac1e80fb", "openfda": {"unii": ["2F5R1A46YW"], "rxcui": ["259306", "403975"], "spl_set_id": ["2846a244-7540-442b-81bc-638e641497ce"], "manufacturer_name": ["Lifestar Pharma LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (70756-702-30)", "package_ndc": "70756-702-30", "marketing_start_date": "20200914"}], "brand_name": "Alosetron", "product_id": "70756-702_6e1e5a99-5018-42e7-8e2c-bcd0ac1e80fb", "dosage_form": "TABLET", "pharm_class": ["Serotonin 3 Receptor Antagonists [MoA]", "Serotonin-3 Receptor Antagonist [EPC]"], "product_ndc": "70756-702", "generic_name": "Alosetron", "labeler_name": "Lifestar Pharma LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Alosetron", "active_ingredients": [{"name": "ALOSETRON HYDROCHLORIDE", "strength": ".5 mg/1"}], "application_number": "ANDA213614", "marketing_category": "ANDA", "marketing_start_date": "20200914", "listing_expiration_date": "20261231"}