cefadroxil

Generic: cefadroxil

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

Drug Facts

Product Profile

Brand Name cefadroxil
Generic Name cefadroxil
Labeler lupin pharmaceuticals, inc.
Dosage Form POWDER, FOR SUSPENSION
Routes
ORAL
Active Ingredients

cefadroxil 250 mg/5mL

Manufacturer
Lupin Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 68180-181
Product ID 68180-181_3818bd15-cf3a-4b07-bef5-57169a33a170
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA065396
Listing Expiration 2026-12-31
Marketing Start 2008-04-23

Pharmacologic Class

Classes
cephalosporin antibacterial [epc] cephalosporins [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 68180181
Hyphenated Format 68180-181

Supplemental Identifiers

RxCUI
105171 309048
UNII
280111G160

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 cefadroxil (source: ndc)
Generic Name cefadroxil (source: ndc)
Application Number ANDA065396 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 250 mg/5mL
source: ndc
Packaging
  • 100 mL in 1 BOTTLE (68180-181-02)
source: ndc

Packages (1)

68180-181-02 100 mL in 1 BOTTLE (68180-181-02)

Ingredients (1)

cefadroxil (250 mg/5mL)

Linked Drug Pages (1)

Cefadroxil ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "3818bd15-cf3a-4b07-bef5-57169a33a170", "openfda": {"unii": ["280111G160"], "rxcui": ["105171", "309048"], "spl_set_id": ["27009a05-4d2b-4618-be76-39f348240eda"], "manufacturer_name": ["Lupin Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 mL in 1 BOTTLE (68180-181-02)", "package_ndc": "68180-181-02", "marketing_start_date": "20080423"}], "brand_name": "Cefadroxil", "product_id": "68180-181_3818bd15-cf3a-4b07-bef5-57169a33a170", "dosage_form": "POWDER, FOR SUSPENSION", "pharm_class": ["Cephalosporin Antibacterial [EPC]", "Cephalosporins [CS]"], "product_ndc": "68180-181", "generic_name": "Cefadroxil", "labeler_name": "Lupin Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cefadroxil", "active_ingredients": [{"name": "CEFADROXIL", "strength": "250 mg/5mL"}], "application_number": "ANDA065396", "marketing_category": "ANDA", "marketing_start_date": "20080423", "listing_expiration_date": "20261231"}