United States · FDA National Drug Code directory

Clindamycin Phosphate

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
51672-4081_503c6717-9dad-2fd5-e063-6294a90a35f6
Product NDC
51672-4081
Form
SOLUTION
Composition / generic term
Clindamycin phosphate
Labeler
Sun Pharmaceutical Industries, Inc.
Marketing category
ANDA
Marketing start / end (source format)
20040331
Source listing expiry
20271231

Source-listed ingredients

  • CLINDAMYCIN PHOSPHATE — 10 mg/mL

These values do not establish equivalence or a dose recommendation.

Packages

  • 1 BOTTLE, WITH APPLICATOR in 1 CARTON (51672-4081-3) / 30 mL in 1 BOTTLE, WITH APPLICATOR · 51672-4081-3
  • 1 BOTTLE, WITH APPLICATOR in 1 CARTON (51672-4081-4) / 60 mL in 1 BOTTLE, WITH APPLICATOR · 51672-4081-4

Source and coverage

Open FDA National Drug Code directory

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.

Browse United States records →