cefdinir

Generic: cefdinir

Labeler: nucare pharmaceuticals,inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name cefdinir
Generic Name cefdinir
Labeler nucare pharmaceuticals,inc.
Dosage Form POWDER, FOR SUSPENSION
Routes
ORAL
Active Ingredients

cefdinir 125 mg/5mL

Manufacturer
NuCare Pharmaceuticals,Inc.

Identifiers & Regulatory

Product NDC 68071-4970
Product ID 68071-4970_1b2e8147-7c01-7d0a-e063-6394a90aeea1
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)
cephalosporin antibacterial [epc]
Chemical Structure
cephalosporins [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 680714970
Hyphenated Format 68071-4970

Supplemental Identifiers

RxCUI
309054
UPC
0368071497069
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 ANDA065473 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 125 mg/5mL
source: ndc
Packaging
  • 60 mL in 1 BOTTLE (68071-4970-6)
source: ndc

Packages (1)

Ingredients (1)

cefdinir (125 mg/5mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "1b2e8147-7c01-7d0a-e063-6394a90aeea1", "openfda": {"nui": ["N0000175488", "M0003827"], "upc": ["0368071497069"], "unii": ["CI0FAO63WC"], "rxcui": ["309054"], "spl_set_id": ["8dfbad95-4dd8-01fd-e053-2a95a90a1de1"], "pharm_class_cs": ["Cephalosporins [CS]"], "pharm_class_epc": ["Cephalosporin Antibacterial [EPC]"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "60 mL in 1 BOTTLE (68071-4970-6)", "package_ndc": "68071-4970-6", "marketing_start_date": "20190718"}], "brand_name": "Cefdinir", "product_id": "68071-4970_1b2e8147-7c01-7d0a-e063-6394a90aeea1", "dosage_form": "POWDER, FOR SUSPENSION", "pharm_class": ["Cephalosporin Antibacterial [EPC]", "Cephalosporins [CS]"], "product_ndc": "68071-4970", "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": "ANDA065473", "marketing_category": "ANDA", "marketing_start_date": "20071214", "listing_expiration_date": "20261231"}