Package 43066-090-25

Brand: prochlorperazine edisylate

Generic: prochlorperazine edisylate
NDC Package

Package Facts

Identity

Package NDC 43066-090-25
Digits Only 4306609025
Product NDC 43066-090
Product ID 43066-090_5894a965-dd6b-4435-b2e5-203a23d4b70e
Description

25 VIAL in 1 CARTON (43066-090-25) / 2 mL in 1 VIAL (43066-090-01)

Marketing

Marketing Status
Marketed Since 2021-05-03
Brand prochlorperazine edisylate
Generic prochlorperazine edisylate
Sample Package No

Linked Drug Pages (1)

PROCHLORPERAZINE EDISYLATE ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "5894a965-dd6b-4435-b2e5-203a23d4b70e", "openfda": {"upc": ["0343066090012"], "unii": ["PG20W5VQZS"], "rxcui": ["2102949"], "spl_set_id": ["11cb37c7-01b4-4223-b2ea-a3695639b80b"], "manufacturer_name": ["Baxter Healthcare Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL in 1 CARTON (43066-090-25)  / 2 mL in 1 VIAL (43066-090-01)", "package_ndc": "43066-090-25", "marketing_start_date": "20210503"}], "brand_name": "PROCHLORPERAZINE EDISYLATE", "product_id": "43066-090_5894a965-dd6b-4435-b2e5-203a23d4b70e", "dosage_form": "INJECTION", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "43066-090", "generic_name": "prochlorperazine edisylate", "labeler_name": "Baxter Healthcare Corporation", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "PROCHLORPERAZINE EDISYLATE", "active_ingredients": [{"name": "PROCHLORPERAZINE EDISYLATE", "strength": "5 mg/mL"}], "application_number": "ANDA214379", "marketing_category": "ANDA", "marketing_start_date": "20210503", "listing_expiration_date": "20261231"}