United States · FDA National Drug Code directory

SILDENAFIL CITRATE

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
75834-240_506bb4eb-697e-9d05-e063-6294a90a8f2c
Product NDC
75834-240
Form
TABLET
Composition / generic term
SILDENAFIL CITRATE
Labeler
NIVAGEN PHARMACEUTICALS, INC.
Marketing category
ANDA
Marketing start / end (source format)
20200904
Source listing expiry
20271231

Source-listed ingredients

  • SILDENAFIL CITRATE — 50 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 1000 TABLET in 1 BOTTLE (75834-240-00) · 75834-240-00
  • 100 TABLET in 1 BOTTLE (75834-240-01) · 75834-240-01
  • 500 TABLET in 1 BOTTLE (75834-240-05) · 75834-240-05
  • 30 TABLET in 1 BOTTLE (75834-240-30) · 75834-240-30

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 CITRATE — United States | Molindra Medicines