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
- 71205-657_fd8ab326-7f1b-42b4-a20c-39ed68e79378
- Product NDC
- 71205-657
- Form
- TABLET
- Composition / generic term
- SILDENAFIL CITRATE
- Labeler
- Proficient Rx LP
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20200904
- Source listing expiry
- 20261231
Source-listed ingredients
- SILDENAFIL CITRATE — 100 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 2 TABLET in 1 BOTTLE (71205-657-02) · 71205-657-02
- 10 TABLET in 1 BOTTLE (71205-657-10) · 71205-657-10
- 1000 TABLET in 1 BOTTLE (71205-657-11) · 71205-657-11
- 20 TABLET in 1 BOTTLE (71205-657-20) · 71205-657-20
- 30 TABLET in 1 BOTTLE (71205-657-30) · 71205-657-30
- 60 TABLET in 1 BOTTLE (71205-657-60) · 71205-657-60
- 90 TABLET in 1 BOTTLE (71205-657-90) · 71205-657-90
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 →