cefprozil

Generic: cefprozil

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

Drug Facts

Product Profile

Brand Name cefprozil
Generic Name cefprozil
Labeler lupin pharmaceuticals, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

cefprozil 500 mg/1

Manufacturer
Lupin Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 68180-404
Product ID 68180-404_b5bc3f77-ca01-4c3f-b8b6-591a3d8f73f4
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA065276
Listing Expiration 2026-12-31
Marketing Start 2005-12-01

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 68180404
Hyphenated Format 68180-404

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 ANDA065276 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 500 mg/1
source: ndc
Packaging
  • 50 TABLET in 1 BOTTLE (68180-404-01)
source: ndc

Packages (1)

68180-404-01 50 TABLET in 1 BOTTLE (68180-404-01)

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": "b5bc3f77-ca01-4c3f-b8b6-591a3d8f73f4", "openfda": {"nui": ["N0000175488", "M0003827"], "unii": ["4W0459ZA4V"], "rxcui": ["197452", "197453"], "spl_set_id": ["14527f4a-ce99-449d-a5a5-9edd7fb28dee"], "pharm_class_cs": ["Cephalosporins [CS]"], "pharm_class_epc": ["Cephalosporin Antibacterial [EPC]"], "manufacturer_name": ["Lupin Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "50 TABLET in 1 BOTTLE (68180-404-01)", "package_ndc": "68180-404-01", "marketing_start_date": "20051201"}], "brand_name": "CEFPROZIL", "product_id": "68180-404_b5bc3f77-ca01-4c3f-b8b6-591a3d8f73f4", "dosage_form": "TABLET", "product_ndc": "68180-404", "generic_name": "CEFPROZIL", "labeler_name": "Lupin Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "CEFPROZIL", "active_ingredients": [{"name": "CEFPROZIL", "strength": "500 mg/1"}], "application_number": "ANDA065276", "marketing_category": "ANDA", "marketing_start_date": "20051201", "listing_expiration_date": "20261231"}