Package 76045-737-10

Brand: haloperidol

Generic: haloperidol lactate
NDC Package

Package Facts

Identity

Package NDC 76045-737-10
Digits Only 7604573710
Product NDC 76045-737
Product ID 76045-737_740165fb-1e22-44ae-bc3e-3b66a6862c1a
Description

24 SYRINGE in 1 CARTON (76045-737-10) / 1 mL in 1 SYRINGE (76045-737-01)

Marketing

Marketing Status
Marketed Since 2019-07-01
Brand haloperidol
Generic haloperidol lactate
Sample Package No

Linked Drug Pages (1)

Haloperidol ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAMUSCULAR"], "spl_id": "740165fb-1e22-44ae-bc3e-3b66a6862c1a", "openfda": {"unii": ["6387S86PK3"], "rxcui": ["1876502"], "spl_set_id": ["a9970612-0ab3-4a8b-ae84-231738d913a4"], "manufacturer_name": ["Fresenius Kabi USA, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "24 SYRINGE in 1 CARTON (76045-737-10)  / 1 mL in 1 SYRINGE (76045-737-01)", "package_ndc": "76045-737-10", "marketing_start_date": "20190701"}], "brand_name": "Haloperidol", "product_id": "76045-737_740165fb-1e22-44ae-bc3e-3b66a6862c1a", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Typical Antipsychotic [EPC]"], "product_ndc": "76045-737", "generic_name": "haloperidol lactate", "labeler_name": "Fresenius Kabi USA, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Haloperidol", "active_ingredients": [{"name": "HALOPERIDOL LACTATE", "strength": "5 mg/mL"}], "application_number": "ANDA210356", "marketing_category": "ANDA", "marketing_start_date": "20190701", "listing_expiration_date": "20261231"}