NDC codes

FDA NDC Directory
Product NDC (as listed)82347-0205Labeler and product segments. Claims need a package NDC.
Product NDC at billing width82347-0205Add the package segment from the table below.
Package NDCs as listed with the FDA, and the 11-digit 5-4-2 form used on claims. The highlighted digit is the added leading zero.
Package NDC11-digit (billing)PackageCopy
82347-0205-4823470205041 FILM in 1 POUCH (82347-0205-4)Marketed from Feb 15, 2026
82347-0205-5823470205054 POUCH in 1 CARTON (82347-0205-5) / 1 FILM in 1 POUCHMarketed from Feb 15, 2026
82347-0205-6823470205068 POUCH in 1 CARTON (82347-0205-6) / 1 FILM in 1 POUCHMarketed from Feb 15, 2026

How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules

Product information

Brand name (proprietary)
Sildenafil
Generic name (nonproprietary)
sildenafil citrate
Active ingredients
Sildenafil citrate — 25 mg/1
Dosage form
Film
Route
Oral
Product type
Prescription drug
Marketing category
NDA — New Drug ApplicationApplication NDA 210858
Marketing start
Listing expires
Other FDA classes
Phosphodiesterase 5 Inhibitors (Mechanism)
Identifiers
Product ID 82347-0205_567bd8f5-2456-8cb2-e063-6394a90ab411SPL ID 567bd8f5-2456-8cb2-e063-6394a90ab411SPL set ID a17a970e-25a2-4807-9644-74e6d2bd2383RxCUI 2735815, 2735822, 2735825, 2735829UNII BW9B0ZE037UPC 0382347021062
Pharmacologic class
Phosphodiesterase 5 Inhibitor

Billing references

What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.

HCPCS codeNo match

No HCPCS code in Med-Code's directory. Oral products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N482347020504 followed by a unit qualifier and the quantity

Package 82347-0205-04. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier

Product label

Current FDA label (SPL), effective .

Indications (excerpt from the label)

1. INDICATION S AND USAGE SILDENAFIL ORAL FILM is indicated for the treatment of erectile dysfunction. SILDENAFIL ORAL FILM is a phosphodiesterase-5 (PDE5) inhibitor indicated for the treatment of erectile dysfunction (ED). ( 1 )

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under NDA 210858

Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.

FDA NDC Directory listings under NDA 210858
ProductStrengthForm · routeLabelerProduct NDC
Sildenafilsildenafil citrateSildenafil citrate 50 mg/1FilmOralYaral Pharma Inc.82347-0210
Sildenafilsildenafil citrateSildenafil citrate 75 mg/1FilmOralYaral Pharma Inc.82347-0215
Sildenafilsildenafil citrateSildenafil citrate 100 mg/1FilmOralYaral Pharma Inc.82347-0220
Vybriquesildenafil citrateSildenafil citrate 50 mg/1FilmOralIBSA Pharma Inc.71858-0210
Vybriquesildenafil citrateSildenafil citrate 25 mg/1FilmOralIBSA Pharma Inc.71858-0205
Vybriquesildenafil citrateSildenafil citrate 75 mg/1FilmOralIBSA Pharma Inc.71858-0215
Vybriquesildenafil citrateSildenafil citrate 100 mg/1FilmOralIBSA Pharma Inc.71858-0220

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