Package 49884-170-04

Brand: sodium phenylbutyrate

Generic: sodium phenylbutyrate tablets, 500 mg
NDC Package

Package Facts

Identity

Package NDC 49884-170-04
Digits Only 4988417004
Product NDC 49884-170
Product ID 49884-170_0aa4a079-431c-407a-a5e5-645a63020119
Description

1 BOTTLE in 1 CARTON (49884-170-04) / 250 TABLET in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 2016-04-29
Brand sodium phenylbutyrate
Generic sodium phenylbutyrate tablets, 500 mg
Sample Package No

Linked Drug Pages (1)

Sodium Phenylbutyrate ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "0aa4a079-431c-407a-a5e5-645a63020119", "openfda": {"upc": ["0349884170042"], "unii": ["NT6K61736T"], "rxcui": ["199369"], "spl_set_id": ["4020b962-eaee-4184-b04b-14ca757c51a1"], "manufacturer_name": ["ENDO USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (49884-170-04)  / 250 TABLET in 1 BOTTLE", "package_ndc": "49884-170-04", "marketing_start_date": "20160429"}], "brand_name": "Sodium Phenylbutyrate", "product_id": "49884-170_0aa4a079-431c-407a-a5e5-645a63020119", "dosage_form": "TABLET", "pharm_class": ["Ammonium Ion Binding Activity [MoA]", "Nitrogen Binding Agent [EPC]"], "product_ndc": "49884-170", "generic_name": "Sodium Phenylbutyrate Tablets, 500 mg", "labeler_name": "ENDO USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sodium Phenylbutyrate", "active_ingredients": [{"name": "SODIUM PHENYLBUTYRATE", "strength": "500 mg/1"}], "application_number": "ANDA204395", "marketing_category": "ANDA", "marketing_start_date": "20160429", "listing_expiration_date": "20261231"}