NDC codes

FDA NDC Directory
Product NDC (as listed)71335-1005Labeler and product segments. Claims need a package NDC.
Product NDC at billing width71335-1005Add 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
71335-1005-17133510050110 TABLET, FILM COATED in 1 BOTTLE (71335-1005-1)Marketed from Oct 14, 2016
71335-1005-27133510050230 TABLET, FILM COATED in 1 BOTTLE (71335-1005-2)Marketed from Oct 14, 2016
71335-1005-3713351005037 TABLET, FILM COATED in 1 BOTTLE (71335-1005-3)Marketed from Oct 14, 2016
71335-1005-47133510050490 TABLET, FILM COATED in 1 BOTTLE (71335-1005-4)Marketed from Oct 14, 2016
71335-1005-57133510050560 TABLET, FILM COATED in 1 BOTTLE (71335-1005-5)Marketed from Oct 14, 2016
71335-1005-67133510050620 TABLET, FILM COATED in 1 BOTTLE (71335-1005-6)Marketed from Oct 14, 2016
71335-1005-771335100507270 TABLET, FILM COATED in 1 BOTTLE (71335-1005-7)Marketed from Oct 14, 2016
71335-1005-87133510050815 TABLET, FILM COATED in 1 BOTTLE (71335-1005-8)Marketed from Oct 14, 2016
71335-1005-97133510050912 TABLET, FILM COATED in 1 BOTTLE (71335-1005-9)Marketed from Oct 14, 2016

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
Active ingredients
Sildenafil citrate — 20 mg/1
Dosage form
Tablet, Film coated
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 203814
Marketing start
Marketing end
Other FDA classes
Phosphodiesterase 5 Inhibitors (Mechanism)
Identifiers
Product ID 71335-1005_7dde9c19-f947-49da-bcd3-01430780e173SPL ID 7dde9c19-f947-49da-bcd3-01430780e173SPL set ID 7c01fd56-5dd6-4728-9f2a-e0f5db810269RxCUI 577033UNII 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

N471335100501 followed by a unit qualifier and the quantity

Package 71335-1005-01. 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 pulmonary arterial hypertension (WHO Group I) in adults to improve exercise ability and delay clinical worsening. The delay in clinical worsening was demonstrated when sildenafil tablets were added to background epoprostenol therapy [ see Clinical Studies (14) ]. Studies establishing effectiveness were short-term (12 to 16 weeks), and included predominately patients with New York Heart Association (NYHA) Functional Class II-III symptoms and idiopathic etiology (71%) or associated with connective tissue disease (CTD) (25%). Limitation of Use: Adding sildenafil to bosentan therapy does not result in any beneficial effect on exercise capacit…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 203814

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

FDA NDC Directory listings under ANDA 203814
ProductStrengthForm · routeLabelerProduct NDC
SildenafilSildenafil citrate 20 mg/1Tablet, Film coatedOralAmerican Health Packaging60687-788
SildenafilSildenafil citrate 20 mg/1Tablet, Film coatedOralNuCare Pharmaceuticals,Inc.68071-5115
SildenafilSildenafil citrate 20 mg/1Tablet, Film coatedOralNuCare Pharmaceuticals, Inc.68071-2072
SildenafilSildenafil citrate 20 mg/1Tablet, Film coatedOralNuCare Pharmaceuticals,Inc.68071-4517
SildenafilSildenafil citrate 20 mg/1Tablet, Film coatedOralMacleods Pharmaceuticals Limited33342-121
SildenafilSildenafil citrate 20 mg/1Tablet, Film coatedOralMacleods Pharmaceuticals Limited33342-536
SildenafilSildenafil citrate 20 mg/1Tablet, Film coatedOralBluePoint Laboratories68001-597
SildenafilSildenafil citrate 20 mg/1Tablet, Film coatedOralAsclemed USA, Inc.76420-061
SildenafilSildenafil citrate 20 mg/1Tablet, Film coatedOralProficient Rx LP63187-813
SildenafilSildenafil citrate 20 mg/1Tablet, Film coatedOralBryant Ranch Prepack71335-1638
SildenafilSildenafil citrate 20 mg/1Tablet, Film coatedOralBluePoint Laboratories68001-363

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