cefdinir
Generic: cefdinir
Labeler: proficient rx lpDrug Facts
Product Profile
Brand Name
cefdinir
Generic Name
cefdinir
Labeler
proficient rx lp
Dosage Form
POWDER, FOR SUSPENSION
Routes
Active Ingredients
cefdinir 250 mg/5mL
Manufacturer
Identifiers & Regulatory
Product NDC
71205-380
Product ID
71205-380_eb67d441-028c-49e6-93b4-2be3b6bc9acf
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)
Chemical Structure
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
71205380
Hyphenated Format
71205-380
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
- 250 mg/5mL
Packaging
- 100 mL in 1 BOTTLE (71205-380-00)
- 60 mL in 1 BOTTLE (71205-380-60)
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "eb67d441-028c-49e6-93b4-2be3b6bc9acf", "openfda": {"nui": ["N0000175488", "M0003827"], "upc": ["0371205380601"], "unii": ["CI0FAO63WC"], "rxcui": ["476576"], "spl_set_id": ["444cd2c4-836d-40d5-a307-d719fe83e763"], "pharm_class_cs": ["Cephalosporins [CS]"], "pharm_class_epc": ["Cephalosporin Antibacterial [EPC]"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "100 mL in 1 BOTTLE (71205-380-00)", "package_ndc": "71205-380-00", "marketing_start_date": "20210603"}, {"sample": false, "description": "60 mL in 1 BOTTLE (71205-380-60)", "package_ndc": "71205-380-60", "marketing_start_date": "20200106"}], "brand_name": "Cefdinir", "product_id": "71205-380_eb67d441-028c-49e6-93b4-2be3b6bc9acf", "dosage_form": "POWDER, FOR SUSPENSION", "pharm_class": ["Cephalosporin Antibacterial [EPC]", "Cephalosporins [CS]"], "product_ndc": "71205-380", "generic_name": "Cefdinir", "labeler_name": "Proficient Rx LP", "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"}