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
- 72865-103_f26fd1e1-7c9e-b45b-e053-2995a90a162d
- Product NDC
- 72865-103
- Form
- TABLET, FILM COATED
- Composition / generic term
- Sildenafil
- Labeler
- XLCARE Pharmaceuticals INC.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20190801
- Source listing expiry
- 20261231
Source-listed ingredients
- SILDENAFIL CITRATE — 100 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET, FILM COATED in 1 BOTTLE (72865-103-01) · 72865-103-01
- 30 TABLET, FILM COATED in 1 BOTTLE (72865-103-30) · 72865-103-30
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 →