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 monohydrate 125 mg/5mL

Manufacturer
NuCare Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 68071-3156
Product ID 68071-3156_2d53fd8c-5f3f-8b3f-e063-6394a90a3ea0
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA065332
Listing Expiration 2026-12-31
Marketing Start 2007-05-08

Pharmacologic Class

Classes
cephalosporin antibacterial [epc] cephalosporins [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 680713156
Hyphenated Format 68071-3156

Supplemental Identifiers

RxCUI
309054
UPC
0368071315660
UNII
6E7SN358SE

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 ANDA065332 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 125 mg/5mL
source: ndc
Packaging
  • 60 mL in 1 BOTTLE (68071-3156-6)
source: ndc

Packages (1)

68071-3156-6 60 mL in 1 BOTTLE (68071-3156-6)

Ingredients (1)

cefdinir monohydrate (125 mg/5mL)

Linked Drug Pages (1)

Cefdinir ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "2d53fd8c-5f3f-8b3f-e063-6394a90a3ea0", "openfda": {"upc": ["0368071315660"], "unii": ["6E7SN358SE"], "rxcui": ["309054"], "spl_set_id": ["4ade94bb-6c39-13cd-e054-00144ff8d46c"], "manufacturer_name": ["NuCare Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "60 mL in 1 BOTTLE (68071-3156-6)", "package_ndc": "68071-3156-6", "marketing_start_date": "20170316"}], "brand_name": "Cefdinir", "product_id": "68071-3156_2d53fd8c-5f3f-8b3f-e063-6394a90a3ea0", "dosage_form": "POWDER, FOR SUSPENSION", "pharm_class": ["Cephalosporin Antibacterial [EPC]", "Cephalosporins [CS]"], "product_ndc": "68071-3156", "generic_name": "Cefdinir", "labeler_name": "NuCare Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cefdinir", "active_ingredients": [{"name": "CEFDINIR MONOHYDRATE", "strength": "125 mg/5mL"}], "application_number": "ANDA065332", "marketing_category": "ANDA", "marketing_start_date": "20070508", "listing_expiration_date": "20261231"}