Package 72572-580-25
Brand: prochlorperazine edisylate
Generic: prochlorperazine edisylatePackage Facts
Identity
Package NDC
72572-580-25
Digits Only
7257258025
Product NDC
72572-580
Description
25 VIAL in 1 CARTON (72572-580-25) / 2 mL in 1 VIAL (72572-580-01)
Marketing
Marketing Status
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": "7395a535-b3fc-4bb8-b2e1-d8c42b9a0509", "openfda": {"unii": ["PG20W5VQZS"], "rxcui": ["314192"], "spl_set_id": ["e3e0c6c5-6b92-40e0-a926-29c64846be93"], "manufacturer_name": ["Civica, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL in 1 CARTON (72572-580-25) / 2 mL in 1 VIAL (72572-580-01)", "package_ndc": "72572-580-25", "marketing_start_date": "20191118"}], "brand_name": "Prochlorperazine Edisylate", "product_id": "72572-580_7395a535-b3fc-4bb8-b2e1-d8c42b9a0509", "dosage_form": "INJECTION", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "72572-580", "generic_name": "Prochlorperazine Edisylate", "labeler_name": "Civica, Inc.", "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": "20191118", "listing_expiration_date": "20261231"}