cefpodoxime proxetil

Generic: cefpodoxime proxetil

Labeler: northstar rx llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name cefpodoxime proxetil
Generic Name cefpodoxime proxetil
Labeler northstar rx llc
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

cefpodoxime proxetil 200 mg/1

Manufacturer
NorthStar Rx LLC

Identifiers & Regulatory

Product NDC 16714-395
Product ID 16714-395_518e9779-a683-436e-a032-c6a0df0a0de2
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA065370
Listing Expiration 2026-12-31
Marketing Start 2007-06-11

Pharmacologic Class

Classes
cephalosporin antibacterial [epc] cephalosporins [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 16714395
Hyphenated Format 16714-395

Supplemental Identifiers

RxCUI
309076 309078
UNII
2TB00A1Z7N

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name cefpodoxime proxetil (source: ndc)
Generic Name cefpodoxime proxetil (source: ndc)
Application Number ANDA065370 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 200 mg/1
source: ndc
Packaging
  • 20 TABLET, FILM COATED in 1 BOTTLE (16714-395-01)
source: ndc

Packages (1)

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

Ingredients (1)

cefpodoxime proxetil (200 mg/1)

Linked Drug Pages (1)

CEFPODOXIME PROXETIL ndc-match (0.9)

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"}