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
- 70710-1716_b42790ec-b9ad-4b34-b98d-dfb8d246eff2
- Product NDC
- 70710-1716
- Form
- POWDER, FOR SUSPENSION
- Composition / generic term
- Sildenafil Citrate
- Labeler
- Zydus Pharmaceuticals (USA) Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20221027
- Source listing expiry
- 20271231
Source-listed ingredients
- SILDENAFIL CITRATE — 10 mg/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 1 BOTTLE, GLASS in 1 CARTON (70710-1716-4) / 112 mL in 1 BOTTLE, GLASS · 70710-1716-4
- 1 BOTTLE, PLASTIC in 1 CARTON (70710-1716-5) / 112 mL in 1 BOTTLE, PLASTIC · 70710-1716-5
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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