Package 68083-436-01

Brand: prochlorperazine edisylate

Generic: prochlorperazine edisylate
NDC Package

Package Facts

Identity

Package NDC 68083-436-01
Digits Only 6808343601
Product NDC 68083-436
Description

1 VIAL in 1 CARTON (68083-436-01) / 10 mL in 1 VIAL

Marketing

Marketing Status
Marketed Since 2021-09-22
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": "868ffb82-fd9b-4157-9e2c-1b76191ac1aa", "openfda": {"upc": ["0368083436018", "0368083435103", "0368083435257"], "unii": ["PG20W5VQZS"], "rxcui": ["2102949"], "spl_set_id": ["a0fd3d58-7470-4d0f-9e6c-84e92c02a97f"], "manufacturer_name": ["Gland Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 CARTON (68083-436-01)  / 10 mL in 1 VIAL", "package_ndc": "68083-436-01", "marketing_start_date": "20210922"}], "brand_name": "Prochlorperazine Edisylate", "product_id": "68083-436_868ffb82-fd9b-4157-9e2c-1b76191ac1aa", "dosage_form": "INJECTION", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "68083-436", "generic_name": "Prochlorperazine Edisylate", "labeler_name": "Gland Pharma Limited", "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": "20210922", "listing_expiration_date": "20261231"}