Package 17856-0091-3

Brand: aluminum hydroxide

Generic: aluminum hydroxide
NDC Package

Package Facts

Identity

Package NDC 17856-0091-3
Digits Only 1785600913
Product NDC 17856-0091
Product ID 17856-0091_4602216a-bb8c-af52-e063-6294a90a380e
Description

30 mL in 1 CUP (17856-0091-3)

Marketing

Marketing Status
Marketed Since 2024-04-16
Brand aluminum hydroxide
Generic aluminum hydroxide
Sample Package No

Linked Drug Pages (1)

Aluminum Hydroxide ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "4602216a-bb8c-af52-e063-6294a90a380e", "openfda": {"unii": ["5QB0T2IUN0"], "rxcui": ["308078"], "spl_set_id": ["60a54d4e-89c2-4329-86bf-a288527f37b5"], "manufacturer_name": ["ATLANTIC BIOLOGICALS CORP."]}, "finished": true, "packaging": [{"sample": false, "description": "30 mL in 1 CUP (17856-0091-3)", "package_ndc": "17856-0091-3", "marketing_start_date": "20240416"}], "brand_name": "Aluminum Hydroxide", "product_id": "17856-0091_4602216a-bb8c-af52-e063-6294a90a380e", "dosage_form": "LIQUID", "product_ndc": "17856-0091", "generic_name": "aluminum hydroxide", "labeler_name": "ATLANTIC BIOLOGICALS CORP.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Aluminum Hydroxide", "active_ingredients": [{"name": "ALUMINUM HYDROXIDE", "strength": "320 mg/5mL"}], "application_number": "M", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20050201", "listing_expiration_date": "20261231"}