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
- 59746-435_4bcef8ac-9715-407e-a23c-ed036c8827c8
- Product NDC
- 59746-435
- Form
- TABLET, FILM COATED
- Composition / generic term
- sildenafil
- Labeler
- Jubilant Cadista Pharmaceuticals Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20260901
- Source listing expiry
- 20271231
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, PLASTIC (59746-435-01) · 59746-435-01
- 100 TABLET, FILM COATED in 1 CARTON (59746-435-03) · 59746-435-03
- 10 TABLET, FILM COATED in 1 BLISTER PACK (59746-435-04) · 59746-435-04
- 500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (59746-435-05) · 59746-435-05
- 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (59746-435-30) · 59746-435-30
- 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (59746-435-90) · 59746-435-90
Source and coverage
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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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