Package 0143-9746-10

Brand: terbutaline sulfate

Generic: terbutaline sulfate
NDC Package

Package Facts

Identity

Package NDC 0143-9746-10
Digits Only 0143974610
Product NDC 0143-9746
Product ID 0143-9746_3e8736f7-de5c-4906-851f-6a10a53866ad
Description

10 VIAL in 1 CARTON (0143-9746-10) / 1 mL in 1 VIAL (0143-9746-01)

Marketing

Marketing Status
Marketed Since 2009-05-20
Brand terbutaline sulfate
Generic terbutaline sulfate
Sample Package No

Linked Drug Pages (1)

Terbutaline Sulfate ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["SUBCUTANEOUS"], "spl_id": "3e8736f7-de5c-4906-851f-6a10a53866ad", "openfda": {"unii": ["576PU70Y8E"], "rxcui": ["857635"], "spl_set_id": ["613df3cb-4d55-4d12-ab08-a932481aaa0b"], "manufacturer_name": ["Hikma Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL in 1 CARTON (0143-9746-10)  / 1 mL in 1 VIAL (0143-9746-01)", "package_ndc": "0143-9746-10", "marketing_start_date": "20090520"}], "brand_name": "Terbutaline Sulfate", "product_id": "0143-9746_3e8736f7-de5c-4906-851f-6a10a53866ad", "dosage_form": "INJECTION", "product_ndc": "0143-9746", "generic_name": "Terbutaline Sulfate", "labeler_name": "Hikma Pharmaceuticals USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Terbutaline Sulfate", "active_ingredients": [{"name": "TERBUTALINE SULFATE", "strength": "1 mg/mL"}], "application_number": "ANDA078630", "marketing_category": "ANDA", "marketing_start_date": "20090520", "listing_expiration_date": "20261231"}