United States · FDA National Drug Code directory

Cefdinir

A source-listed medicine record.

Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.

Medicine identity

Source reference
0781-2176_977d4566-20b3-4909-ad00-6cbea017798d
Product NDC
0781-2176
Form
CAPSULE
Composition / generic term
Cefdinir
Labeler
Sandoz Inc
Marketing category
ANDA
Marketing start / end (source format)
20070406
Source listing expiry
20261231

Source-listed ingredients

  • CEFDINIR — 300 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 100 CAPSULE in 1 BOTTLE (0781-2176-01) · 0781-2176-01
  • 60 CAPSULE in 1 BOTTLE (0781-2176-60) · 0781-2176-60
  • 3 CARTON in 1 CARTON (0781-2176-64) / 1 BLISTER PACK in 1 CARTON / 10 CAPSULE in 1 BLISTER PACK · 0781-2176-64
  • 5 BLISTER PACK in 1 CARTON (0781-2176-69) / 10 CAPSULE in 1 BLISTER PACK · 0781-2176-69

Source and coverage

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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.

Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.

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