Package 49884-006-04

Brand: sodium phenylbutyrate

Generic: sodium phenylbutyrate
NDC Package

Package Facts

Identity

Package NDC 49884-006-04
Digits Only 4988400604
Product NDC 49884-006
Description

1 BOTTLE in 1 CARTON (49884-006-04) / 250 g in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 2016-08-31
Brand sodium phenylbutyrate
Generic sodium phenylbutyrate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "f2c8509e-be24-4c67-b50e-7096ae15dd2a", "openfda": {"upc": ["0349884006044"], "unii": ["NT6K61736T"], "rxcui": ["984105"], "spl_set_id": ["639f5c7e-9f6d-47fb-a417-2be076176a78"], "manufacturer_name": ["ENDO USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (49884-006-04)  / 250 g in 1 BOTTLE", "package_ndc": "49884-006-04", "marketing_start_date": "20160831"}], "brand_name": "Sodium Phenylbutyrate", "product_id": "49884-006_f2c8509e-be24-4c67-b50e-7096ae15dd2a", "dosage_form": "POWDER", "pharm_class": ["Ammonium Ion Binding Activity [MoA]", "Nitrogen Binding Agent [EPC]"], "product_ndc": "49884-006", "generic_name": "Sodium Phenylbutyrate", "labeler_name": "ENDO USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sodium Phenylbutyrate", "active_ingredients": [{"name": "SODIUM PHENYLBUTYRATE", "strength": ".94 g/g"}], "application_number": "ANDA203918", "marketing_category": "ANDA", "marketing_start_date": "20160831", "listing_expiration_date": "20261231"}