Package 0781-3056-70
Brand: isoniazid
Generic: isoniazidPackage Facts
Identity
Package NDC
0781-3056-70
Digits Only
0781305670
Product NDC
0781-3056
Description
1 VIAL, MULTI-DOSE in 1 CARTON (0781-3056-70) / 10 mL in 1 VIAL, MULTI-DOSE
Marketing
Marketing Status
Brand
isoniazid
Generic
isoniazid
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAMUSCULAR"], "spl_id": "66f2f4a4-1479-450c-8834-89cd29b08f2b", "openfda": {"nui": ["N0000175483"], "unii": ["V83O1VOZ8L"], "rxcui": ["204430"], "spl_set_id": ["77795c31-1cdf-4a20-b4a1-cd15f5b310f1"], "pharm_class_epc": ["Antimycobacterial [EPC]"], "manufacturer_name": ["Sandoz Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, MULTI-DOSE in 1 CARTON (0781-3056-70) / 10 mL in 1 VIAL, MULTI-DOSE", "package_ndc": "0781-3056-70", "marketing_start_date": "20060119"}], "brand_name": "Isoniazid", "product_id": "0781-3056_66f2f4a4-1479-450c-8834-89cd29b08f2b", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Antimycobacterial [EPC]"], "product_ndc": "0781-3056", "generic_name": "Isoniazid", "labeler_name": "Sandoz Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Isoniazid", "active_ingredients": [{"name": "ISONIAZID", "strength": "100 mg/mL"}], "application_number": "ANDA040648", "marketing_category": "ANDA", "marketing_start_date": "20060119", "listing_expiration_date": "20261231"}