NDC codes

FDA NDC Directory
Product NDC (as listed)71858-0215Labeler and product segments. Claims need a package NDC.
Product NDC at billing width71858-0215Add 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
71858-0215-171858021501718580215012 POUCH in 1 CARTON (71858-0215-1) / 1 FILM in 1 POUCHMarketed from Feb 15, 2026 · Sample package
71858-0215-271858021502718580215021 FILM in 1 POUCH (71858-0215-2)Marketed from Feb 15, 2026 · Sample package
71858-0215-471858021504718580215041 FILM in 1 POUCH (71858-0215-4)Marketed from Feb 15, 2026
71858-0215-571858021505718580215054 POUCH in 1 CARTON (71858-0215-5) / 1 FILM in 1 POUCHMarketed from Feb 15, 2026
71858-0215-671858021506718580215068 POUCH in 1 CARTON (71858-0215-6) / 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)
Vybrique
Generic name (nonproprietary)
sildenafil citrate
Active ingredients
Sildenafil citrate — 75 mg/1
Dosage form
Film
Route
Oral
Labeler
IBSA Pharma Inc.NDC labeler code 71858
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 71858-0215_56160b33-eaca-0312-e063-6394a90a4319SPL ID 56160b33-eaca-0312-e063-6394a90a4319SPL set ID 9213fec1-e0c0-4ef7-9718-d97922a3f4d8RxCUI 2735815, 2735821, 2735822, 2735824, 2735825, 2735827, 2735829, 2735831UNII BW9B0ZE037
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

N471858021501 followed by a unit qualifier and the quantity

Package 71858-0215-01. 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 VYBRIQUE TM is indicated for the treatment of erectile dysfunction. VYBRIQUE 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)

About NDC 71858-0215

What is NDC 71858-0215?
71858-0215 is the product NDC for Vybrique (sildenafil citrate), Sildenafil citrate 75 mg/1 film, listed with the FDA by IBSA Pharma Inc.. It has 5 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Vybrique (Sildenafil citrate).
What is the active ingredient?
Sildenafil citrate.
Who is the labeler?
IBSA Pharma Inc., NDC labeler code 71858. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Vybrique?
3 other product NDCs are listed under this name. See all Vybrique NDCs.
Is there a related HCPCS / J-code?
Not in Med-Code's curated HCPCS directory. See Billing references above.

Other finished products listed under the same name: strengths, forms and labelers.

Other Vybrique NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Vybriquesildenafil citrateSildenafil citrate 25 mg/1FilmOralIBSA Pharma Inc.71858-020571858-0205-0271858-0205-0471858-0205-05+1 more
Vybriquesildenafil citrateSildenafil citrate 50 mg/1FilmOralIBSA Pharma Inc.71858-021071858-0210-0171858-0210-0271858-0210-04+2 more
Vybriquesildenafil citrateSildenafil citrate 100 mg/1FilmOralIBSA Pharma Inc.71858-022071858-0220-0171858-0220-0271858-0220-04+2 more

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 25 mg/1FilmOralYaral Pharma Inc.82347-0205
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 25 mg/1FilmOralIBSA Pharma Inc.71858-0205
Vybriquesildenafil citrateSildenafil citrate 50 mg/1FilmOralIBSA Pharma Inc.71858-0210
Vybriquesildenafil citrateSildenafil citrate 100 mg/1FilmOralIBSA Pharma Inc.71858-0220

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