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
68071-2602_3ab073e6-dfb5-0795-e063-6294a90ab146
Product NDC
68071-2602
Form
TABLET
Composition / generic term
Sildenafil
Labeler
NuCare Pharmaceuticals,Inc.
Marketing category
ANDA
Marketing start / end (source format)
20180504
Source listing expiry
20261231

Source-listed ingredients

  • SILDENAFIL CITRATE — 20 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 10 TABLET in 1 BOTTLE (68071-2602-1) · 68071-2602-1
  • 30 TABLET in 1 BOTTLE (68071-2602-3) · 68071-2602-3

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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