cefpodoxime proxetil

Generic: cefpodoxime proxetil

Labeler: nucare pharmaceuticals,inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name cefpodoxime proxetil
Generic Name cefpodoxime proxetil
Labeler nucare pharmaceuticals,inc.
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

cefpodoxime proxetil 200 mg/1

Manufacturer
NuCare Pharmaceuticals,Inc.

Identifiers & Regulatory

Product NDC 68071-3441
Product ID 68071-3441_2d80b340-7ddc-adf0-e063-6294a90af485
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA210568
Listing Expiration 2026-12-31
Marketing Start 2023-02-13

Pharmacologic Class

Classes
cephalosporin antibacterial [epc] cephalosporins [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 680713441
Hyphenated Format 68071-3441

Supplemental Identifiers

RxCUI
309078
UPC
0368071344127
UNII
2TB00A1Z7N

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 ANDA210568 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 200 mg/1
source: ndc
Packaging
  • 20 TABLET, FILM COATED in 1 BOTTLE (68071-3441-2)
source: ndc

Packages (1)

68071-3441-2 20 TABLET, FILM COATED in 1 BOTTLE (68071-3441-2)

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": "2d80b340-7ddc-adf0-e063-6294a90af485", "openfda": {"upc": ["0368071344127"], "unii": ["2TB00A1Z7N"], "rxcui": ["309078"], "spl_set_id": ["fe827f61-9336-72e7-e053-6394a90af75f"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "20 TABLET, FILM COATED in 1 BOTTLE (68071-3441-2)", "package_ndc": "68071-3441-2", "marketing_start_date": "20230619"}], "brand_name": "Cefpodoxime Proxetil", "product_id": "68071-3441_2d80b340-7ddc-adf0-e063-6294a90af485", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cephalosporin Antibacterial [EPC]", "Cephalosporins [CS]"], "product_ndc": "68071-3441", "generic_name": "Cefpodoxime Proxetil", "labeler_name": "NuCare Pharmaceuticals,Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cefpodoxime Proxetil", "active_ingredients": [{"name": "CEFPODOXIME PROXETIL", "strength": "200 mg/1"}], "application_number": "ANDA210568", "marketing_category": "ANDA", "marketing_start_date": "20230213", "listing_expiration_date": "20261231"}