Package 76329-3302-1

Brand: dextrose monohydrate

Generic: dextrose monohydrate
NDC Package

Package Facts

Identity

Package NDC 76329-3302-1
Digits Only 7632933021
Product NDC 76329-3302
Description

1 SYRINGE in 1 CARTON (76329-3302-1) / 50 mL in 1 SYRINGE

Marketing

Marketing Status
Marketed Since 2021-11-11
Brand dextrose monohydrate
Generic dextrose monohydrate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "45b366a9-6c0c-4643-9951-4ff880b29c83", "openfda": {"unii": ["LX22YL083G"], "rxcui": ["727517"], "spl_set_id": ["fcc7ac79-cd70-4f03-a4de-f051f9ca1f7d"], "manufacturer_name": ["International Medication Systems, Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 SYRINGE in 1 CARTON (76329-3302-1)  / 50 mL in 1 SYRINGE", "package_ndc": "76329-3302-1", "marketing_start_date": "20211111"}], "brand_name": "Dextrose Monohydrate", "product_id": "76329-3302_45b366a9-6c0c-4643-9951-4ff880b29c83", "dosage_form": "INJECTION, SOLUTION", "product_ndc": "76329-3302", "generic_name": "Dextrose Monohydrate", "labeler_name": "International Medication Systems, Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Dextrose Monohydrate", "active_ingredients": [{"name": "DEXTROSE MONOHYDRATE", "strength": "25 g/50mL"}], "application_number": "ANDA203451", "marketing_category": "ANDA", "marketing_start_date": "20211111", "listing_expiration_date": "20261231"}