Package 54482-054-01

Brand: matulane

Generic: procarbazine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 54482-054-01
Digits Only 5448205401
Product NDC 54482-054
Description

100 CAPSULE in 1 BOTTLE (54482-054-01)

Marketing

Marketing Status
Marketed Since 1985-12-27
Brand matulane
Generic procarbazine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "caa705fa-c467-49b5-a7cb-ae2c8b872a86", "openfda": {"unii": ["XH0NPH5ZX8"], "rxcui": ["207588", "314167"], "spl_set_id": ["1aa75a3a-18c9-49e1-91a6-293d0b7da756"], "manufacturer_name": ["Leadiant Biosciences, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (54482-054-01)", "package_ndc": "54482-054-01", "marketing_start_date": "19851227"}], "brand_name": "Matulane", "product_id": "54482-054_caa705fa-c467-49b5-a7cb-ae2c8b872a86", "dosage_form": "CAPSULE", "pharm_class": ["Alkylating Activity [MoA]", "Alkylating Drug [EPC]"], "product_ndc": "54482-054", "generic_name": "procarbazine hydrochloride", "labeler_name": "Leadiant Biosciences, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Matulane", "active_ingredients": [{"name": "PROCARBAZINE HYDROCHLORIDE", "strength": "50 mg/1"}], "application_number": "NDA016785", "marketing_category": "NDA", "marketing_start_date": "19851227", "listing_expiration_date": "20261231"}