Package 0641-6225-10
Brand: Prochlorperazine Edisylate
Generic: Prochlorperazine EdisylatePackage Facts
Identity
Package NDC
0641-6225-10
Digits Only
0641622510
Product NDC
0641-6225
Description
10 SYRINGE in 1 CARTON (0641-6225-10) / 2 mL in 1 SYRINGE (0641-6225-01)
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": "f3e74a48-3072-44f3-9370-ee8a4213585f", "openfda": {"unii": ["PG20W5VQZS"], "rxcui": ["2633008"], "spl_set_id": ["b3c5c1b7-310a-4658-bd01-b88b7334b591"], "manufacturer_name": ["Hikma Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 SYRINGE in 1 CARTON (0641-6225-10) / 2 mL in 1 SYRINGE (0641-6225-01)", "package_ndc": "0641-6225-10", "marketing_start_date": "20230102"}], "brand_name": "Prochlorperazine Edisylate", "product_id": "0641-6225_f3e74a48-3072-44f3-9370-ee8a4213585f", "dosage_form": "INJECTION", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "0641-6225", "generic_name": "Prochlorperazine Edisylate", "labeler_name": "Hikma Pharmaceuticals USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Prochlorperazine Edisylate", "active_ingredients": [{"name": "PROCHLORPERAZINE EDISYLATE", "strength": "5 mg/mL"}], "application_number": "ANDA213630", "marketing_category": "ANDA", "marketing_start_date": "20230102", "listing_expiration_date": "20261231"}