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
- 68071-3862_521e7b08-8bdb-c4be-e063-6394a90a9124
- Product NDC
- 68071-3862
- Form
- TABLET, FILM COATED
- Composition / generic term
- SILDENAFIL
- Labeler
- NuCare Pharmaceuticals, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20180611
- Source listing expiry
- 20271231
Source-listed ingredients
- SILDENAFIL CITRATE — 100 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 10 TABLET, FILM COATED in 1 BOTTLE (68071-3862-1) · 68071-3862-1
- 15 TABLET, FILM COATED in 1 BOTTLE (68071-3862-5) · 68071-3862-5
- 60 TABLET, FILM COATED in 1 BOTTLE (68071-3862-6) · 68071-3862-6
- 90 TABLET, FILM COATED in 1 BOTTLE (68071-3862-9) · 68071-3862-9
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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