Package 72266-204-10
Brand: prochlorperazine edisylate
Generic: prochlorperazine edisylatePackage Facts
Identity
Package NDC
72266-204-10
Digits Only
7226620410
Product NDC
72266-204
Description
10 VIAL in 1 CARTON (72266-204-10) / 2 mL in 1 VIAL (72266-204-01)
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": "24fdbe72-a9c4-6144-e063-6394a90ac10d", "openfda": {"unii": ["PG20W5VQZS"], "rxcui": ["2102949"], "spl_set_id": ["f793cdb3-9fd8-79e1-e053-6394a90ae08b"], "manufacturer_name": ["FOSUN PHARMA USA INC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL in 1 CARTON (72266-204-10) / 2 mL in 1 VIAL (72266-204-01)", "package_ndc": "72266-204-10", "marketing_start_date": "20230501"}], "brand_name": "Prochlorperazine Edisylate", "product_id": "72266-204_24fdbe72-a9c4-6144-e063-6394a90ac10d", "dosage_form": "INJECTION", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "72266-204", "generic_name": "Prochlorperazine Edisylate", "labeler_name": "FOSUN PHARMA USA INC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Prochlorperazine Edisylate", "active_ingredients": [{"name": "PROCHLORPERAZINE EDISYLATE", "strength": "5 mg/mL"}], "application_number": "ANDA214107", "marketing_category": "ANDA", "marketing_start_date": "20230501", "listing_expiration_date": "20261231"}