Package 54348-989-06

Brand: prochlorperazine

Generic: prochlorperazine
NDC Package

Package Facts

Identity

Package NDC 54348-989-06
Digits Only 5434898906
Product NDC 54348-989
Product ID 54348-989_eaa6022b-bb02-9383-e053-2995a90abe88
Description

1 BOTTLE in 1 BOX (54348-989-06) / 6 TABLET in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 2019-07-11
Brand prochlorperazine
Generic prochlorperazine
Sample Package No

Linked Drug Pages (1)

Prochlorperazine ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "eaa6022b-bb02-9383-e053-2995a90abe88", "openfda": {"unii": ["I1T8O1JTL6"], "rxcui": ["312635"], "spl_set_id": ["383744db-ba57-478a-8041-2ecc26d3e1ec"], "manufacturer_name": ["PharmPak, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 BOX (54348-989-06)  / 6 TABLET in 1 BOTTLE", "package_ndc": "54348-989-06", "marketing_start_date": "20190711"}], "brand_name": "Prochlorperazine", "product_id": "54348-989_eaa6022b-bb02-9383-e053-2995a90abe88", "dosage_form": "TABLET", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "54348-989", "generic_name": "PROCHLORPERAZINE", "labeler_name": "PharmPak, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Prochlorperazine", "active_ingredients": [{"name": "PROCHLORPERAZINE MALEATE", "strength": "5 mg/1"}], "application_number": "ANDA040268", "marketing_category": "ANDA", "marketing_start_date": "20190711", "listing_expiration_date": "20261231"}