NDC codes

FDA NDC Directory
Product NDC (as listed)62332-235Labeler and product segments. Claims need a package NDC.
Product NDC at billing width62332-0235Add 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
62332-235-04623320235044 BLISTER PACK in 1 CARTON (62332-235-04) / 4 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACKMarketed from Nov 20, 2018

How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 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)
Vardenafil
Generic name (nonproprietary)
vardenafil
Active ingredients
Vardenafil hydrochloride trihydrate — 10 mg/1
Dosage form
Tablet, Orally disintegrating
Route
Oral
Labeler
Alembic Pharmaceuticals Inc.NDC labeler code 62332
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 208324
Marketing start
Listing expires
Other FDA classes
Phosphodiesterase 5 Inhibitors (Mechanism)
Identifiers
Product ID 62332-235_33bb2a69-79e4-49bb-9388-97367b428639SPL ID 33bb2a69-79e4-49bb-9388-97367b428639SPL set ID 0ce4eb7b-fa50-441d-ae71-eb33dca27926RxCUI 996179UNII 5M8S2CU0TS
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

N462332023504 followed by a unit qualifier and the quantity

Package 62332-0235-04. 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)

Vardenafil hydrochloride orally disintegrating tablets are indicated for the treatment of erectile dysfunction. • Vardenafil hydrochloride orally disintegrating tablets are phosphodiesterase 5 (PDE5) inhibitor indicated for the treatment of erectile dysfunction. ( 1 ).

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 62332-235

What is NDC 62332-235?
62332-235 is the product NDC for Vardenafil, Vardenafil hydrochloride trihydrate 10 mg/1 tablet, orally disintegrating, listed with the FDA by Alembic Pharmaceuticals Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Vardenafil.
What is the active ingredient?
Vardenafil hydrochloride trihydrate.
Who is the labeler?
Alembic Pharmaceuticals Inc., NDC labeler code 62332. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Vardenafil?
11 other product NDCs are listed under this name. See all Vardenafil 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 Vardenafil NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
VardenafilVardenafil hydrochloride trihydrate 10 mg/1Tablet, Orally disintegratingOralAlembic Pharmaceuticals Limited46708-23546708-0235-04
VardenafilVardenafil hydrochloride trihydrate 2.5 mg/1Tablet, Film coatedOralZydus Pharmaceuticals USA Inc.70710-106870710-1068-0170710-1068-0370710-1068-09
VardenafilVardenafil hydrochloride trihydrate 5 mg/1Tablet, Film coatedOralZydus Pharmaceuticals USA Inc.70710-106970710-1069-0170710-1069-0370710-1069-09
VardenafilVardenafil hydrochloride trihydrate 10 mg/1Tablet, Film coatedOralZydus Pharmaceuticals USA Inc.70710-107070710-1070-0170710-1070-0370710-1070-09
VardenafilVardenafil hydrochloride trihydrate 20 mg/1Tablet, Film coatedOralZydus Pharmaceuticals USA Inc.70710-107170710-1071-0170710-1071-0370710-1071-09
VardenafilVardenafil hydrochloride trihydrate 2.5 mg/1Tablet, Film coatedOralZydus Lifesciences Limited70771-104770771-1047-0170771-1047-0370771-1047-09
VardenafilVardenafil hydrochloride trihydrate 5 mg/1Tablet, Film coatedOralZydus Lifesciences Limited70771-104870771-1048-0170771-1048-0370771-1048-09
VardenafilVardenafil hydrochloride trihydrate 10 mg/1Tablet, Film coatedOralZydus Lifesciences Limited70771-104970771-1049-0170771-1049-0370771-1049-09
VardenafilVardenafil hydrochloride trihydrate 20 mg/1Tablet, Film coatedOralZydus Lifesciences Limited70771-105070771-1050-0170771-1050-0370771-1050-09
VardenafilVardenafil hydrochloride trihydrate 20 mg/1Tablet, Film coatedOralAphena Pharma Solutions - Tennessee, LLC71610-47771610-0477-0271610-0477-0471610-0477-06+1 more

All 12 Vardenafil NDCs

Other NDCs under ANDA 208324

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

FDA NDC Directory listings under ANDA 208324
ProductStrengthForm · routeLabelerProduct NDC
VardenafilVardenafil hydrochloride trihydrate 10 mg/1Tablet, Orally disintegratingOralAlembic Pharmaceuticals Limited46708-235

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