Package 0074-1040-08

Brand: survanta

Generic: beractant
NDC Package

Package Facts

Identity

Package NDC 0074-1040-08
Digits Only 0074104008
Product NDC 0074-1040
Product ID 0074-1040_6ff1e6a7-1578-4e78-b34f-eb204b23554c
Description

1 VIAL, SINGLE-USE in 1 CARTON (0074-1040-08) / 8 mL in 1 VIAL, SINGLE-USE

Marketing

Marketing Status
Marketed Since 1991-07-01
Brand survanta
Generic beractant
Sample Package No

Linked Drug Pages (1)

Survanta ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ENDOTRACHEAL"], "spl_id": "6ff1e6a7-1578-4e78-b34f-eb204b23554c", "openfda": {"nui": ["N0000008294", "N0000175778", "N0000000079"], "unii": ["S866O45PIG"], "rxcui": ["259034", "861715"], "spl_set_id": ["7ef9e3a5-fc39-4ae1-0dad-6b47a1684635"], "pharm_class_pe": ["Alveolar Surface Tension Reduction [PE]"], "pharm_class_epc": ["Surfactant [EPC]"], "pharm_class_moa": ["Surfactant Activity [MoA]"], "manufacturer_name": ["AbbVie Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, SINGLE-USE in 1 CARTON (0074-1040-04)  / 4 mL in 1 VIAL, SINGLE-USE", "package_ndc": "0074-1040-04", "marketing_start_date": "19910701"}, {"sample": false, "description": "1 VIAL, SINGLE-USE in 1 CARTON (0074-1040-08)  / 8 mL in 1 VIAL, SINGLE-USE", "package_ndc": "0074-1040-08", "marketing_start_date": "19910701"}], "brand_name": "Survanta", "product_id": "0074-1040_6ff1e6a7-1578-4e78-b34f-eb204b23554c", "dosage_form": "SUSPENSION", "product_ndc": "0074-1040", "generic_name": "Beractant", "labeler_name": "AbbVie Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Survanta", "active_ingredients": [{"name": "BERACTANT", "strength": "25 mg/mL"}], "application_number": "BLA020032", "marketing_category": "BLA", "marketing_start_date": "19910701", "listing_expiration_date": "20261231"}