cefdinir

Generic: cefdinir

Labeler: direct rx
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name cefdinir
Generic Name cefdinir
Labeler direct rx
Dosage Form POWDER, FOR SUSPENSION
Routes
ORAL
Active Ingredients

cefdinir 250 mg/5mL

Manufacturer
DIRECT RX

Identifiers & Regulatory

Product NDC 72189-186
Product ID 72189-186_2c4ea169-07c6-6bde-e063-6394a90a0890
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA065473
Listing Expiration 2026-12-31
Marketing Start 2021-04-12

Pharmacologic Class

Established (EPC)
cephalosporin antibacterial [epc]
Chemical Structure
cephalosporins [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72189186
Hyphenated Format 72189-186

Supplemental Identifiers

RxCUI
309054 476576
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
  • 250 mg/5mL
source: ndc
Packaging
  • 60 mL in 1 BOTTLE (72189-186-32)
source: ndc

Packages (1)

72189-186-32 60 mL in 1 BOTTLE (72189-186-32)

Ingredients (1)

cefdinir (250 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": "2c4ea169-07c6-6bde-e063-6394a90a0890", "openfda": {"nui": ["N0000175488", "M0003827"], "unii": ["CI0FAO63WC"], "rxcui": ["309054", "476576"], "spl_set_id": ["982d0f53-20bc-1cb4-e053-2995a90ad33c"], "pharm_class_cs": ["Cephalosporins [CS]"], "pharm_class_epc": ["Cephalosporin Antibacterial [EPC]"], "manufacturer_name": ["DIRECT RX"]}, "finished": true, "packaging": [{"sample": false, "description": "60 mL in 1 BOTTLE (72189-186-32)", "package_ndc": "72189-186-32", "marketing_start_date": "20210412"}], "brand_name": "CEFDINIR", "product_id": "72189-186_2c4ea169-07c6-6bde-e063-6394a90a0890", "dosage_form": "POWDER, FOR SUSPENSION", "pharm_class": ["Cephalosporin Antibacterial [EPC]", "Cephalosporins [CS]"], "product_ndc": "72189-186", "generic_name": "CEFDINIR", "labeler_name": "DIRECT RX", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "CEFDINIR", "active_ingredients": [{"name": "CEFDINIR", "strength": "250 mg/5mL"}], "application_number": "ANDA065473", "marketing_category": "ANDA", "marketing_start_date": "20210412", "listing_expiration_date": "20261231"}