United States · FDA National Drug Code directory

Nafcillin

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
63323-328_89168d2d-2dc0-3f50-e053-2a95a90a31be
Product NDC
63323-328
Form
INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Composition / generic term
NAFCILLIN SODIUM
Labeler
Fresenius Kabi USA, LLC
Marketing category
ANDA
Marketing start / end (source format)
20110630
Source listing expiry
20261231

Source-listed ingredients

  • NAFCILLIN SODIUM — 2 g/8mL

These values do not establish equivalence or a dose recommendation.

Packages

  • 10 VIAL in 1 CARTON (63323-328-20) / 8 mL in 1 VIAL (63323-328-21) · 63323-328-20

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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