cefdinir
Generic: cefdinir
Labeler: a-s medication solutionsDrug Facts
Product Profile
Brand Name
cefdinir
Generic Name
cefdinir
Labeler
a-s medication solutions
Dosage Form
POWDER, FOR SUSPENSION
Routes
Active Ingredients
cefdinir 250 mg/5mL
Manufacturer
Identifiers & Regulatory
Product NDC
50090-2735
Product ID
50090-2735_664df642-b804-4457-b571-d45e9cd547be
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA065473
Listing Expiration
2026-12-31
Marketing Start
2007-12-14
Pharmacologic Class
Established (EPC)
Chemical Structure
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
500902735
Hyphenated Format
50090-2735
Supplemental Identifiers
RxCUI
UNII
NUI
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
ANDA065473 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 250 mg/5mL
Packaging
- 1 BOTTLE in 1 CARTON (50090-2735-0) / 60 mL in 1 BOTTLE
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "664df642-b804-4457-b571-d45e9cd547be", "openfda": {"nui": ["N0000175488", "M0003827"], "unii": ["CI0FAO63WC"], "rxcui": ["476576"], "spl_set_id": ["beeb9480-f9f9-44ae-93f3-6f4da81888f5"], "pharm_class_cs": ["Cephalosporins [CS]"], "pharm_class_epc": ["Cephalosporin Antibacterial [EPC]"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (50090-2735-0) / 60 mL in 1 BOTTLE", "package_ndc": "50090-2735-0", "marketing_start_date": "20161229"}], "brand_name": "Cefdinir", "product_id": "50090-2735_664df642-b804-4457-b571-d45e9cd547be", "dosage_form": "POWDER, FOR SUSPENSION", "pharm_class": ["Cephalosporin Antibacterial [EPC]", "Cephalosporins [CS]"], "product_ndc": "50090-2735", "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": "ANDA065473", "marketing_category": "ANDA", "marketing_start_date": "20071214", "listing_expiration_date": "20261231"}