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
- 65862-690_98bf3100-9a4e-45d5-9f6b-1fa1a06b26b8
- Product NDC
- 65862-690
- Form
- TABLET, FILM COATED
- Composition / generic term
- Sildenafil
- Labeler
- Aurobindo Pharma Limited
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20180611
- Source listing expiry
- 20261231
Source-listed ingredients
- SILDENAFIL CITRATE — 50 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET, FILM COATED in 1 BOTTLE (65862-690-01) · 65862-690-01
- 500 TABLET, FILM COATED in 1 BOTTLE (65862-690-05) · 65862-690-05
- 30 TABLET, FILM COATED in 1 BOTTLE (65862-690-30) · 65862-690-30
- 1000 TABLET, FILM COATED in 1 BOTTLE (65862-690-99) · 65862-690-99
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 →