cefdinir
Generic: cefdinir
Labeler: preferred pharmaceuticals inc.Drug Facts
Product Profile
Brand Name
cefdinir
Generic Name
cefdinir
Labeler
preferred pharmaceuticals inc.
Dosage Form
POWDER, FOR SUSPENSION
Routes
Active Ingredients
cefdinir 250 mg/5mL
Manufacturer
Identifiers & Regulatory
Product NDC
68788-8062
Product ID
68788-8062_a4846977-d5df-4dc2-aba0-f20b8c94bb85
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA210534
Listing Expiration
2026-12-31
Marketing Start
2021-08-13
Pharmacologic Class
Established (EPC)
Chemical Structure
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
687888062
Hyphenated Format
68788-8062
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
ANDA210534 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 250 mg/5mL
Packaging
- 100 mL in 1 BOTTLE (68788-8062-1)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "a4846977-d5df-4dc2-aba0-f20b8c94bb85", "openfda": {"nui": ["N0000175488", "M0003827"], "unii": ["CI0FAO63WC"], "rxcui": ["476576"], "spl_set_id": ["43131b6b-6cda-4bb6-b73b-9cfeb314d4e2"], "pharm_class_cs": ["Cephalosporins [CS]"], "pharm_class_epc": ["Cephalosporin Antibacterial [EPC]"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 mL in 1 BOTTLE (68788-8062-1)", "package_ndc": "68788-8062-1", "marketing_start_date": "20210813"}], "brand_name": "cefdinir", "product_id": "68788-8062_a4846977-d5df-4dc2-aba0-f20b8c94bb85", "dosage_form": "POWDER, FOR SUSPENSION", "pharm_class": ["Cephalosporin Antibacterial [EPC]", "Cephalosporins [CS]"], "product_ndc": "68788-8062", "generic_name": "cefdinir", "labeler_name": "Preferred Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "cefdinir", "active_ingredients": [{"name": "CEFDINIR", "strength": "250 mg/5mL"}], "application_number": "ANDA210534", "marketing_category": "ANDA", "marketing_start_date": "20210813", "listing_expiration_date": "20261231"}