cefdinir

Generic: cefdinir

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

Drug Facts

Product Profile

Brand Name cefdinir
Generic Name cefdinir
Labeler teva pharmaceuticals usa, inc.
Dosage Form POWDER, FOR SUSPENSION
Routes
ORAL
Active Ingredients

cefdinir monohydrate 125 mg/5mL

Manufacturer
Teva Pharmaceuticals USA, Inc.

Identifiers & Regulatory

Product NDC 0093-4136
Product ID 0093-4136_7f269e55-b085-4315-807a-e425f0189b2c
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA065332
Listing Expiration 2026-12-31
Marketing Start 2007-05-08

Pharmacologic Class

Classes
cephalosporin antibacterial [epc] cephalosporins [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 00934136
Hyphenated Format 0093-4136

Supplemental Identifiers

RxCUI
309054 476576
UNII
6E7SN358SE

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 cefdinir (source: ndc)
Generic Name cefdinir (source: ndc)
Application Number ANDA065332 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 125 mg/5mL
source: ndc
Packaging
  • 60 mL in 1 BOTTLE (0093-4136-64)
  • 100 mL in 1 BOTTLE (0093-4136-73)
source: ndc

Packages (2)

Ingredients (1)

cefdinir monohydrate (125 mg/5mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "7f269e55-b085-4315-807a-e425f0189b2c", "openfda": {"unii": ["6E7SN358SE"], "rxcui": ["309054", "476576"], "spl_set_id": ["a1f49fe1-b511-4f6b-a912-8ae8662d95a5"], "manufacturer_name": ["Teva Pharmaceuticals USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "60 mL in 1 BOTTLE (0093-4136-64)", "package_ndc": "0093-4136-64", "marketing_start_date": "20070508"}, {"sample": false, "description": "100 mL in 1 BOTTLE (0093-4136-73)", "package_ndc": "0093-4136-73", "marketing_start_date": "20070508"}], "brand_name": "Cefdinir", "product_id": "0093-4136_7f269e55-b085-4315-807a-e425f0189b2c", "dosage_form": "POWDER, FOR SUSPENSION", "pharm_class": ["Cephalosporin Antibacterial [EPC]", "Cephalosporins [CS]"], "product_ndc": "0093-4136", "generic_name": "Cefdinir", "labeler_name": "Teva Pharmaceuticals USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cefdinir", "active_ingredients": [{"name": "CEFDINIR MONOHYDRATE", "strength": "125 mg/5mL"}], "application_number": "ANDA065332", "marketing_category": "ANDA", "marketing_start_date": "20070508", "listing_expiration_date": "20261231"}