cefixime

Generic: cefixime

Labeler: aurobindo pharma limited
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name cefixime
Generic Name cefixime
Labeler aurobindo pharma limited
Dosage Form POWDER, FOR SUSPENSION
Routes
ORAL
Active Ingredients

cefixime 200 mg/5mL

Manufacturer
Aurobindo Pharma Limited

Identifiers & Regulatory

Product NDC 65862-752
Product ID 65862-752_141b12c3-31de-4ca7-ac89-d864975846ab
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA204835
Listing Expiration 2026-12-31
Marketing Start 2015-04-14

Pharmacologic Class

Classes
cephalosporin antibacterial [epc] cephalosporins [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 65862752
Hyphenated Format 65862-752

Supplemental Identifiers

RxCUI
309058 419849
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 ANDA204835 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 200 mg/5mL
source: ndc
Packaging
  • 50 mL in 1 BOTTLE (65862-752-50)
  • 75 mL in 1 BOTTLE (65862-752-75)
source: ndc

Packages (2)

Ingredients (1)

cefixime (200 mg/5mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "141b12c3-31de-4ca7-ac89-d864975846ab", "openfda": {"unii": ["97I1C92E55"], "rxcui": ["309058", "419849"], "spl_set_id": ["068e6edd-a5fe-40d8-8dcf-ac82b78dced4"], "manufacturer_name": ["Aurobindo Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "50 mL in 1 BOTTLE (65862-752-50)", "package_ndc": "65862-752-50", "marketing_start_date": "20150414"}, {"sample": false, "description": "75 mL in 1 BOTTLE (65862-752-75)", "package_ndc": "65862-752-75", "marketing_start_date": "20150414"}], "brand_name": "Cefixime", "product_id": "65862-752_141b12c3-31de-4ca7-ac89-d864975846ab", "dosage_form": "POWDER, FOR SUSPENSION", "pharm_class": ["Cephalosporin Antibacterial [EPC]", "Cephalosporins [CS]"], "product_ndc": "65862-752", "generic_name": "cefixime", "labeler_name": "Aurobindo Pharma Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cefixime", "active_ingredients": [{"name": "CEFIXIME", "strength": "200 mg/5mL"}], "application_number": "ANDA204835", "marketing_category": "ANDA", "marketing_start_date": "20150414", "listing_expiration_date": "20261231"}