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
71610-679_f4dbdb1b-c31d-4418-abd9-883eef04d5bd
Product NDC
71610-679
Form
TABLET
Composition / generic term
SILDENAFIL
Labeler
Aphena Pharma Solutions - Tennessee, LLC
Marketing category
ANDA
Marketing start / end (source format)
20220701
Source listing expiry
20261231

Source-listed ingredients

  • SILDENAFIL CITRATE — 50 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 2 TABLET in 1 BOTTLE (71610-679-02) · 71610-679-02
  • 4 TABLET in 1 BOTTLE (71610-679-04) · 71610-679-04
  • 6 TABLET in 1 BOTTLE (71610-679-06) · 71610-679-06

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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SILDENAFIL — United States | Molindra Medicines