NDC codes

FDA NDC Directory
Product NDC (as listed)59746-436Labeler and product segments. Claims need a package NDC.
Product NDC at billing width59746-0436Add 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
59746-436-015974604360159746043601100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (59746-436-01)Marketed from Sep 1, 2026
59746-436-035974604360359746043603100 TABLET, FILM COATED in 1 CARTON (59746-436-03)Marketed from Sep 1, 2026
59746-436-04597460436045974604360410 TABLET, FILM COATED in 1 BLISTER PACK (59746-436-04)Marketed from Sep 1, 2026
59746-436-055974604360559746043605500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (59746-436-05)Marketed from Sep 1, 2026
59746-436-30597460436305974604363030 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (59746-436-30)Marketed from Sep 1, 2026
59746-436-90597460436905974604369090 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (59746-436-90)Marketed from Sep 1, 2026

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)
Sildenafil
Generic name (nonproprietary)
sildenafil
Active ingredients
Sildenafil citrate — 100 mg/1
Dosage form
Tablet, Film coated
Route
Oral
Labeler
Jubilant Cadista Pharmaceuticals Inc.NDC labeler code 59746
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 201156
Marketing start
Listing expires
Other FDA classes
Phosphodiesterase 5 Inhibitors (Mechanism)
Identifiers
Product ID 59746-436_4bcef8ac-9715-407e-a23c-ed036c8827c8SPL ID 4bcef8ac-9715-407e-a23c-ed036c8827c8SPL set ID 1ed2420b-478a-ca9c-0330-85c845acdd32RxCUI 312950, 314228, 314229UNII BW9B0ZE037UPC 0359746436308, 0359746436018, 0359746435301, 0359746434304, 0359746435011
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

N459746043601 followed by a unit qualifier and the quantity

Package 59746-0436-01. 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)

Sildenafil tablets are indicated for the treatment of erectile dysfunction. Sildenafil tablets are 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 59746-436

What is NDC 59746-436?
59746-436 is the product NDC for Sildenafil, Sildenafil citrate 100 mg/1 tablet, film coated, listed with the FDA by Jubilant Cadista Pharmaceuticals Inc.. It has 6 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Sildenafil.
What is the active ingredient?
Sildenafil citrate.
Who is the labeler?
Jubilant Cadista Pharmaceuticals Inc., NDC labeler code 59746. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Sildenafil?
150 other product NDCs are listed under this name. See all Sildenafil 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 Sildenafil NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
SildenafilSildenafil citrate 25 mg/1Tablet, Film coatedOralJubilant Cadista Pharmaceuticals Inc.59746-43459746-0434-0359746-0434-0459746-0434-05+2 more
SildenafilSildenafil citrate 50 mg/1Tablet, Film coatedOralJubilant Cadista Pharmaceuticals Inc.59746-43559746-0435-0159746-0435-0359746-0435-04+3 more
SildenafilSildenafil citrate 20 mg/1TabletOralREMEDYREPACK INC.70518-459670518-4596-00
Sildenafilsildenafil citrateSildenafil citrate 25 mg/1FilmOralYaral Pharma Inc.82347-020582347-0205-0482347-0205-0582347-0205-06
Sildenafilsildenafil citrateSildenafil citrate 50 mg/1FilmOralYaral Pharma Inc.82347-021082347-0210-0482347-0210-0582347-0210-06
Sildenafilsildenafil citrateSildenafil citrate 75 mg/1FilmOralYaral Pharma Inc.82347-021582347-0215-0482347-0215-0582347-0215-06
Sildenafilsildenafil citrateSildenafil citrate 100 mg/1FilmOralYaral Pharma Inc.82347-022082347-0220-0482347-0220-0582347-0220-06
SildenafilSildenafil citrate 20 mg/1Tablet, Film coatedOralGolden State Medical Supply, Inc.51407-98751407-0987-90
SildenafilSildenafil citrate 20 mg/1TabletOralAvKARE42291-93742291-0937-90
SildenafilSildenafil citrate 20 mg/1Tablet, Film coatedOralJubilant Cadista Pharmaceuticals Inc.59746-47159746-0471-0559746-0471-1059746-0471-90

All 151 Sildenafil NDCs

Other NDCs under ANDA 201156

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

FDA NDC Directory listings under ANDA 201156
ProductStrengthForm · routeLabelerProduct NDC
SildenafilSildenafil citrate 25 mg/1Tablet, Film coatedOralJubilant Cadista Pharmaceuticals Inc.59746-434
SildenafilSildenafil citrate 50 mg/1Tablet, Film coatedOralJubilant Cadista Pharmaceuticals Inc.59746-435

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