cefprozil

Generic: cefprozil

Labeler: a-s medication solutions
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name cefprozil
Generic Name cefprozil
Labeler a-s medication solutions
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

cefprozil 500 mg/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-1710
Product ID 50090-1710_ff9d76a8-9edd-4344-85dc-ee245e26d376
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA065340
Listing Expiration 2026-12-31
Marketing Start 2007-05-24

Pharmacologic Class

Established (EPC)
cephalosporin antibacterial [epc]
Chemical Structure
cephalosporins [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 500901710
Hyphenated Format 50090-1710

Supplemental Identifiers

RxCUI
197453
UNII
4W0459ZA4V
NUI
N0000175488 M0003827

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 cefprozil (source: ndc)
Generic Name cefprozil (source: ndc)
Application Number ANDA065340 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 500 mg/1
source: ndc
Packaging
  • 20 TABLET, FILM COATED in 1 BOTTLE (50090-1710-0)
source: ndc

Packages (1)

50090-1710-0 20 TABLET, FILM COATED in 1 BOTTLE (50090-1710-0)

Ingredients (1)

cefprozil (500 mg/1)

Linked Drug Pages (1)

Cefprozil ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "ff9d76a8-9edd-4344-85dc-ee245e26d376", "openfda": {"nui": ["N0000175488", "M0003827"], "unii": ["4W0459ZA4V"], "rxcui": ["197453"], "spl_set_id": ["d5d28d57-1f3c-4c80-ad78-0f67635f5428"], "pharm_class_cs": ["Cephalosporins [CS]"], "pharm_class_epc": ["Cephalosporin Antibacterial [EPC]"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "20 TABLET, FILM COATED in 1 BOTTLE (50090-1710-0)", "package_ndc": "50090-1710-0", "marketing_start_date": "20150225"}], "brand_name": "Cefprozil", "product_id": "50090-1710_ff9d76a8-9edd-4344-85dc-ee245e26d376", "dosage_form": "TABLET, FILM COATED", "product_ndc": "50090-1710", "generic_name": "Cefprozil", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cefprozil", "active_ingredients": [{"name": "CEFPROZIL", "strength": "500 mg/1"}], "application_number": "ANDA065340", "marketing_category": "ANDA", "marketing_start_date": "20070524", "listing_expiration_date": "20261231"}