Package 70069-371-25
Brand: prochlorperazine edisylate
Generic: prochlorperazine edisylatePackage Facts
Identity
Package NDC
70069-371-25
Digits Only
7006937125
Product NDC
70069-371
Description
25 VIAL in 1 CARTON (70069-371-25) / 2 mL in 1 VIAL (70069-371-01)
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": "2d2a447e-bfc4-42dc-b581-31c224ad24b1", "openfda": {"upc": ["0370069371015", "0370069371251", "0370069371107"], "unii": ["PG20W5VQZS"], "rxcui": ["2102949"], "spl_set_id": ["d382e3d4-3175-42f2-b9eb-d9a7b97cbbfc"], "manufacturer_name": ["Somerset Therapeutics, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL in 1 CARTON (70069-371-25) / 2 mL in 1 VIAL (70069-371-01)", "package_ndc": "70069-371-25", "marketing_start_date": "20241010"}], "brand_name": "Prochlorperazine Edisylate", "product_id": "70069-371_2d2a447e-bfc4-42dc-b581-31c224ad24b1", "dosage_form": "INJECTION", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "70069-371", "generic_name": "Prochlorperazine Edisylate", "labeler_name": "Somerset Therapeutics, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Prochlorperazine Edisylate", "active_ingredients": [{"name": "PROCHLORPERAZINE EDISYLATE", "strength": "5 mg/mL"}], "application_number": "ANDA212257", "marketing_category": "ANDA", "marketing_start_date": "20241010", "listing_expiration_date": "20261231"}