cefixime

Generic: cefixime

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

Drug Facts

Product Profile

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

cefixime 200 mg/5mL

Manufacturer
Lupin Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 68180-407
Product ID 68180-407_735f86f4-369c-4f5a-adbe-7dacea2e27b4
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA065355
Listing Expiration 2026-12-31
Marketing Start 2015-04-24

Pharmacologic Class

Classes
cephalosporin antibacterial [epc] cephalosporins [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 68180407
Hyphenated Format 68180-407

Supplemental Identifiers

RxCUI
309058 409823 419849
UPC
0368180423089 0368180407034 0368180416081 0368180416111
UNII
97I1C92E55

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 cefixime (source: ndc)
Generic Name cefixime (source: ndc)
Application Number ANDA065355 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 200 mg/5mL
source: ndc
Packaging
  • 50 mL in 1 BOTTLE (68180-407-03)
  • 75 mL in 1 BOTTLE (68180-407-04)
source: ndc

Packages (2)

68180-407-03 50 mL in 1 BOTTLE (68180-407-03) 68180-407-04 75 mL in 1 BOTTLE (68180-407-04)

Ingredients (1)

cefixime (200 mg/5mL)

Linked Drug Pages (1)

CEFIXIME ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "735f86f4-369c-4f5a-adbe-7dacea2e27b4", "openfda": {"upc": ["0368180423089", "0368180407034", "0368180416081", "0368180416111"], "unii": ["97I1C92E55"], "rxcui": ["309058", "409823", "419849"], "spl_set_id": ["6d68dbd9-7d75-4ff1-91db-79ff8ae879ec"], "manufacturer_name": ["Lupin Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "50 mL in 1 BOTTLE (68180-407-03)", "package_ndc": "68180-407-03", "marketing_start_date": "20150424"}, {"sample": false, "description": "75 mL in 1 BOTTLE (68180-407-04)", "package_ndc": "68180-407-04", "marketing_start_date": "20150424"}], "brand_name": "CEFIXIME", "product_id": "68180-407_735f86f4-369c-4f5a-adbe-7dacea2e27b4", "dosage_form": "POWDER, FOR SUSPENSION", "pharm_class": ["Cephalosporin Antibacterial [EPC]", "Cephalosporins [CS]"], "product_ndc": "68180-407", "generic_name": "CEFIXIME", "labeler_name": "Lupin Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "CEFIXIME", "active_ingredients": [{"name": "CEFIXIME", "strength": "200 mg/5mL"}], "application_number": "ANDA065355", "marketing_category": "ANDA", "marketing_start_date": "20150424", "listing_expiration_date": "20261231"}