Package 0338-1075-02

Brand: dobutamine hydrochloride in dextrose

Generic: dobutamine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0338-1075-02
Digits Only 0338107502
Product NDC 0338-1075
Description

18 BAG in 1 CARTON (0338-1075-02) / 250 mL in 1 BAG

Marketing

Marketing Status
Marketed Since 1993-09-27
Brand dobutamine hydrochloride in dextrose
Generic dobutamine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "34c787c1-46f7-4264-951d-c88a34dca533", "openfda": {"unii": ["0WR771DJXV"], "rxcui": ["309985", "309986", "309987"], "spl_set_id": ["6b17b98b-e06d-42ed-925f-69aa2699dead"], "manufacturer_name": ["Baxter Healthcare Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "18 BAG in 1 CARTON (0338-1075-02)  / 250 mL in 1 BAG", "package_ndc": "0338-1075-02", "marketing_start_date": "19930927"}], "brand_name": "Dobutamine Hydrochloride in Dextrose", "product_id": "0338-1075_34c787c1-46f7-4264-951d-c88a34dca533", "dosage_form": "INJECTION", "pharm_class": ["Adrenergic beta-Agonists [MoA]", "beta-Adrenergic Agonist [EPC]"], "product_ndc": "0338-1075", "generic_name": "Dobutamine Hydrochloride", "labeler_name": "Baxter Healthcare Corporation", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Dobutamine Hydrochloride in Dextrose", "active_ingredients": [{"name": "DOBUTAMINE HYDROCHLORIDE", "strength": "200 mg/100mL"}], "application_number": "NDA020255", "marketing_category": "NDA", "marketing_start_date": "19930927", "listing_expiration_date": "20271231"}