Package 16714-390-01

Brand: cefadroxil

Generic: cefadroxil
NDC Package

Package Facts

Identity

Package NDC 16714-390-01
Digits Only 1671439001
Product NDC 16714-390
Description

75 mL in 1 BOTTLE (16714-390-01)

Marketing

Marketing Status
Marketed Since 2013-04-25
Brand cefadroxil
Generic cefadroxil
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "323b9a4d-c8fc-4fdb-bba4-834468a0a770", "openfda": {"upc": ["0316714390024", "0316714389011"], "unii": ["280111G160"], "rxcui": ["105171", "309048"], "spl_set_id": ["30bb3686-87b4-4676-9ff5-e20deb8bff9d"], "manufacturer_name": ["NorthStar Rx LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "75 mL in 1 BOTTLE (16714-390-01)", "package_ndc": "16714-390-01", "marketing_start_date": "20130425"}, {"sample": false, "description": "100 mL in 1 BOTTLE (16714-390-02)", "package_ndc": "16714-390-02", "marketing_start_date": "20130425"}], "brand_name": "Cefadroxil", "product_id": "16714-390_323b9a4d-c8fc-4fdb-bba4-834468a0a770", "dosage_form": "POWDER, FOR SUSPENSION", "pharm_class": ["Cephalosporin Antibacterial [EPC]", "Cephalosporins [CS]"], "product_ndc": "16714-390", "generic_name": "Cefadroxil", "labeler_name": "NorthStar Rx LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cefadroxil", "active_ingredients": [{"name": "CEFADROXIL", "strength": "500 mg/5mL"}], "application_number": "ANDA065349", "marketing_category": "ANDA", "marketing_start_date": "20130425", "listing_expiration_date": "20261231"}