Package 16714-395-01

Brand: cefpodoxime proxetil

Generic: cefpodoxime proxetil
NDC Package

Package Facts

Identity

Package NDC 16714-395-01
Digits Only 1671439501
Product NDC 16714-395
Product ID 16714-395_518e9779-a683-436e-a032-c6a0df0a0de2
Description

20 TABLET, FILM COATED in 1 BOTTLE (16714-395-01)

Marketing

Marketing Status
Marketed Since 2007-06-11
Brand cefpodoxime proxetil
Generic cefpodoxime proxetil
Sample Package No

Linked Drug Pages (1)

CEFPODOXIME PROXETIL ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "518e9779-a683-436e-a032-c6a0df0a0de2", "openfda": {"unii": ["2TB00A1Z7N"], "rxcui": ["309076", "309078"], "spl_set_id": ["4587a7c1-cd6c-4946-a0dd-fcfe0c8504b9"], "manufacturer_name": ["NorthStar Rx LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "20 TABLET, FILM COATED in 1 BOTTLE (16714-395-01)", "package_ndc": "16714-395-01", "marketing_start_date": "20070611"}], "brand_name": "CEFPODOXIME PROXETIL", "product_id": "16714-395_518e9779-a683-436e-a032-c6a0df0a0de2", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cephalosporin Antibacterial [EPC]", "Cephalosporins [CS]"], "product_ndc": "16714-395", "generic_name": "CEFPODOXIME PROXETIL", "labeler_name": "NorthStar Rx LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "CEFPODOXIME PROXETIL", "active_ingredients": [{"name": "CEFPODOXIME PROXETIL", "strength": "200 mg/1"}], "application_number": "ANDA065370", "marketing_category": "ANDA", "marketing_start_date": "20070611", "listing_expiration_date": "20261231"}