Package 46287-009-01

Brand: isoniazid

Generic: isoniazid
NDC Package

Package Facts

Identity

Package NDC 46287-009-01
Digits Only 4628700901
Product NDC 46287-009
Product ID 46287-009_b4455fa7-39e3-41a5-9a5b-5ff7c490de89
Description

473 mL in 1 BOTTLE (46287-009-01)

Marketing

Marketing Status
Marketed Since 1983-11-11
Brand isoniazid
Generic isoniazid
Sample Package No

Linked Drug Pages (1)

Isoniazid ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "b4455fa7-39e3-41a5-9a5b-5ff7c490de89", "openfda": {"nui": ["N0000175483"], "unii": ["V83O1VOZ8L"], "rxcui": ["105292"], "spl_set_id": ["db8a3ae7-fb5b-47a9-a9f7-f57cd90501c2"], "pharm_class_epc": ["Antimycobacterial [EPC]"], "manufacturer_name": ["CMP Pharma, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "473 mL in 1 BOTTLE (46287-009-01)", "package_ndc": "46287-009-01", "marketing_start_date": "19831111"}], "brand_name": "Isoniazid", "product_id": "46287-009_b4455fa7-39e3-41a5-9a5b-5ff7c490de89", "dosage_form": "SOLUTION", "pharm_class": ["Antimycobacterial [EPC]"], "product_ndc": "46287-009", "generic_name": "isoniazid", "labeler_name": "CMP Pharma, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Isoniazid", "active_ingredients": [{"name": "ISONIAZID", "strength": "50 mg/5mL"}], "application_number": "ANDA088235", "marketing_category": "ANDA", "marketing_start_date": "19831111", "listing_expiration_date": "20261231"}