cefdinir

Generic: cefdinir

Labeler: a-s medication solutions
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name cefdinir
Generic Name cefdinir
Labeler a-s medication solutions
Dosage Form POWDER, FOR SUSPENSION
Routes
ORAL
Active Ingredients

cefdinir 250 mg/5mL

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-3723
Product ID 50090-3723_f7220add-1b4c-47b8-91da-98dd62cd7d3e
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA065259
Listing Expiration 2026-12-31
Marketing Start 2007-05-07

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 500903723
Hyphenated Format 50090-3723

Supplemental Identifiers

RxCUI
476576
UNII
CI0FAO63WC
NUI
N0000175488 M0003827

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 ANDA065259 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 250 mg/5mL
source: ndc
Packaging
  • 100 mL in 1 BOTTLE (50090-3723-0)
source: ndc

Packages (1)

Ingredients (1)

cefdinir (250 mg/5mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "f7220add-1b4c-47b8-91da-98dd62cd7d3e", "openfda": {"nui": ["N0000175488", "M0003827"], "unii": ["CI0FAO63WC"], "rxcui": ["476576"], "spl_set_id": ["17b4e82f-4169-4ab9-bd4a-79781a71e160"], "pharm_class_cs": ["Cephalosporins [CS]"], "pharm_class_epc": ["Cephalosporin Antibacterial [EPC]"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "100 mL in 1 BOTTLE (50090-3723-0)", "package_ndc": "50090-3723-0", "marketing_start_date": "20181025"}], "brand_name": "Cefdinir", "product_id": "50090-3723_f7220add-1b4c-47b8-91da-98dd62cd7d3e", "dosage_form": "POWDER, FOR SUSPENSION", "pharm_class": ["Cephalosporin Antibacterial [EPC]", "Cephalosporins [CS]"], "product_ndc": "50090-3723", "generic_name": "Cefdinir", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cefdinir", "active_ingredients": [{"name": "CEFDINIR", "strength": "250 mg/5mL"}], "application_number": "ANDA065259", "marketing_category": "ANDA", "marketing_start_date": "20070507", "listing_expiration_date": "20261231"}