cefprozil

Generic: cefprozil

Labeler: ascend laboratories, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name cefprozil
Generic Name cefprozil
Labeler ascend laboratories, llc
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

cefprozil 500 mg/1

Manufacturer
Ascend Laboratories, LLC

Identifiers & Regulatory

Product NDC 67877-243
Product ID 67877-243_2e36bf51-2cc6-441a-ad40-6d752e3e4e9b
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA090857
Listing Expiration 2026-12-31
Marketing Start 2025-01-20

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 67877243
Hyphenated Format 67877-243

Supplemental Identifiers

RxCUI
197452 197453
UNII
4W0459ZA4V
NUI
N0000175488 M0003827

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 cefprozil (source: ndc)
Generic Name cefprozil (source: ndc)
Application Number ANDA090857 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 500 mg/1
source: ndc
Packaging
  • 50 TABLET, FILM COATED in 1 BOTTLE (67877-243-50)
source: ndc

Packages (1)

Ingredients (1)

cefprozil (500 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2e36bf51-2cc6-441a-ad40-6d752e3e4e9b", "openfda": {"nui": ["N0000175488", "M0003827"], "unii": ["4W0459ZA4V"], "rxcui": ["197452", "197453"], "spl_set_id": ["dc3e9cae-6f4f-4045-a11e-2fbf7f94c3c0"], "pharm_class_cs": ["Cephalosporins [CS]"], "pharm_class_epc": ["Cephalosporin Antibacterial [EPC]"], "manufacturer_name": ["Ascend Laboratories, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "50 TABLET, FILM COATED in 1 BOTTLE (67877-243-50)", "package_ndc": "67877-243-50", "marketing_start_date": "20250120"}], "brand_name": "Cefprozil", "product_id": "67877-243_2e36bf51-2cc6-441a-ad40-6d752e3e4e9b", "dosage_form": "TABLET, FILM COATED", "product_ndc": "67877-243", "generic_name": "Cefprozil", "labeler_name": "Ascend Laboratories, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cefprozil", "active_ingredients": [{"name": "CEFPROZIL", "strength": "500 mg/1"}], "application_number": "ANDA090857", "marketing_category": "ANDA", "marketing_start_date": "20250120", "listing_expiration_date": "20261231"}