cefdinir
Generic: cefdinir
Labeler: nucare pharmaceuticals, inc.Drug Facts
Product Profile
Brand Name
cefdinir
Generic Name
cefdinir
Labeler
nucare pharmaceuticals, inc.
Dosage Form
POWDER, FOR SUSPENSION
Routes
Active Ingredients
cefdinir 125 mg/5mL
Manufacturer
Identifiers & Regulatory
Product NDC
68071-3806
Product ID
68071-3806_2fb43adf-3e71-176f-e063-6394a90a29e0
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA065259
Listing Expiration
2026-12-31
Marketing Start
2006-05-31
Pharmacologic Class
Established (EPC)
Chemical Structure
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
680713806
Hyphenated Format
68071-3806
Supplemental Identifiers
RxCUI
UPC
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
ANDA065259 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 125 mg/5mL
Packaging
- 100 mL in 1 BOTTLE (68071-3806-1)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2fb43adf-3e71-176f-e063-6394a90a29e0", "openfda": {"nui": ["N0000175488", "M0003827"], "upc": ["0368071380613"], "unii": ["CI0FAO63WC"], "rxcui": ["309054"], "spl_set_id": ["2fb43fbe-2c4b-1df9-e063-6394a90a9913"], "pharm_class_cs": ["Cephalosporins [CS]"], "pharm_class_epc": ["Cephalosporin Antibacterial [EPC]"], "manufacturer_name": ["NuCare Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 mL in 1 BOTTLE (68071-3806-1)", "package_ndc": "68071-3806-1", "marketing_start_date": "20250306"}], "brand_name": "Cefdinir", "product_id": "68071-3806_2fb43adf-3e71-176f-e063-6394a90a29e0", "dosage_form": "POWDER, FOR SUSPENSION", "pharm_class": ["Cephalosporin Antibacterial [EPC]", "Cephalosporins [CS]"], "product_ndc": "68071-3806", "generic_name": "Cefdinir", "labeler_name": "NuCare Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cefdinir", "active_ingredients": [{"name": "CEFDINIR", "strength": "125 mg/5mL"}], "application_number": "ANDA065259", "marketing_category": "ANDA", "marketing_start_date": "20060531", "listing_expiration_date": "20261231"}