United States · FDA National Drug Code directory

Sildenafil

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
0591-4050_4c7d4ea0-d3b7-4a20-b5d6-09207153aaad
Product NDC
0591-4050
Form
POWDER, FOR SUSPENSION
Composition / generic term
Sildenafil
Labeler
Actavis Pharma, Inc.
Marketing category
ANDA
Marketing start / end (source format)
20200817
Source listing expiry
20261231

Source-listed ingredients

  • SILDENAFIL CITRATE — 10 mg/mL

These values do not establish equivalence or a dose recommendation.

Packages

  • 1 BOTTLE in 1 CARTON (0591-4050-94) / 112 mL in 1 BOTTLE · 0591-4050-94

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.

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