Package 51662-1558-3

Brand: prochlorperazine edisylate

Generic: prochlorperazine edisylate
NDC Package

Package Facts

Identity

Package NDC 51662-1558-3
Digits Only 5166215583
Product NDC 51662-1558
Description

25 POUCH in 1 CASE (51662-1558-3) / 1 VIAL in 1 POUCH (51662-1558-2) / 2 mL in 1 VIAL

Marketing

Marketing Status
Marketed Since 2022-06-15
Brand prochlorperazine edisylate
Generic prochlorperazine edisylate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "10358f91-4227-7e42-e063-6394a90a62de", "openfda": {"upc": ["0323155294316"], "unii": ["PG20W5VQZS"], "rxcui": ["2102949"], "spl_set_id": ["e181c18d-32a8-587e-e053-2995a90acc5b"], "manufacturer_name": ["HF Acquisition Co LLC, DBA HealthFirst"]}, "finished": true, "packaging": [{"sample": false, "description": "25 POUCH in 1 CASE (51662-1558-3)  / 1 VIAL in 1 POUCH (51662-1558-2)  / 2 mL in 1 VIAL", "package_ndc": "51662-1558-3", "marketing_start_date": "20220615"}], "brand_name": "PROCHLORPERAZINE EDISYLATE", "product_id": "51662-1558_10358f91-4227-7e42-e063-6394a90a62de", "dosage_form": "INJECTION", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "51662-1558", "generic_name": "PROCHLORPERAZINE EDISYLATE", "labeler_name": "HF Acquisition Co LLC, DBA HealthFirst", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "PROCHLORPERAZINE EDISYLATE", "active_ingredients": [{"name": "PROCHLORPERAZINE EDISYLATE", "strength": "5 mg/mL"}], "application_number": "ANDA089903", "marketing_category": "ANDA", "marketing_start_date": "20220615", "listing_expiration_date": "20261231"}