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
- 75834-241_506bb4eb-697e-9d05-e063-6294a90a8f2c
- Product NDC
- 75834-241
- 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 — 100 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 1000 TABLET in 1 BOTTLE (75834-241-00) · 75834-241-00
- 100 TABLET in 1 BOTTLE (75834-241-01) · 75834-241-01
- 500 TABLET in 1 BOTTLE (75834-241-05) · 75834-241-05
- 30 TABLET in 1 BOTTLE (75834-241-30) · 75834-241-30
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.
Browse United States records →