Package 80725-250-01

Brand: humatin

Generic: paromomycin sulfate
NDC Package

Package Facts

Identity

Package NDC 80725-250-01
Digits Only 8072525001
Product NDC 80725-250
Product ID 80725-250_4b33337a-4e4b-42f3-923f-5b61f02fc463
Description

100 CAPSULE in 1 BOTTLE (80725-250-01)

Marketing

Marketing Status
Marketed Since 2021-04-08
Brand humatin
Generic paromomycin sulfate
Sample Package No

Linked Drug Pages (1)

Humatin ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "4b33337a-4e4b-42f3-923f-5b61f02fc463", "openfda": {"upc": ["0380725250011"], "unii": ["845NU6GJPS"], "rxcui": ["207347", "314184"], "spl_set_id": ["a725f022-ec3c-430d-8021-96c861b9893c"], "manufacturer_name": ["Waylis Therapeutics LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (80725-250-01)", "package_ndc": "80725-250-01", "marketing_start_date": "20210408"}], "brand_name": "Humatin", "product_id": "80725-250_4b33337a-4e4b-42f3-923f-5b61f02fc463", "dosage_form": "CAPSULE", "pharm_class": ["Antiprotozoal [EPC]"], "product_ndc": "80725-250", "generic_name": "PAROMOMYCIN SULFATE", "labeler_name": "Waylis Therapeutics LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Humatin", "active_ingredients": [{"name": "PAROMOMYCIN SULFATE", "strength": "250 mg/1"}], "application_number": "ANDA065173", "marketing_category": "ANDA", "marketing_start_date": "20210408", "listing_expiration_date": "20261231"}