What is NDC 76420-061?

76420-061 is the product NDC for Sildenafil, Sildenafil citrate 20 mg/1 tablet, film coated, listed with the FDA by Asclemed USA, Inc.. It has 3 package NDCs, shown above in 10- and 11-digit form.

Asclemed USA, Inc., NDC labeler code 76420. 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.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Sildenafil NDC 76420-061 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)76420-061Labeler and product segments. Claims need a package NDC.

Product NDC at billing width76420-0061Add 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 NDC	11-digit (billing)	Package
76420-061-30	7642000613076420006130	30 TABLET, FILM COATED in 1 BOTTLE (76420-061-30)Marketed from Dec 10, 2019
76420-061-60	7642000616076420006160	60 TABLET, FILM COATED in 1 BOTTLE (76420-061-60)Marketed from Aug 31, 2022
76420-061-90	7642000619076420006190	90 TABLET, FILM COATED in 1 BOTTLE (76420-061-90)Marketed from Dec 10, 2019

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 — 20 mg/1
Dosage form: Tablet, Film coated
Route: Oral
Labeler: Asclemed USA, Inc.NDC labeler code 76420
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 203814
Marketing start: Jan 3, 2014
Listing expires: Dec 31, 2027
Other FDA classes: Phosphodiesterase 5 Inhibitors (Mechanism)
Identifiers: Product ID 76420-061_e785ec65-b5e8-693c-e053-2995a90aa9e7SPL ID e785ec65-b5e8-693c-e053-2995a90aa9e7SPL set ID 06571775-b651-4e23-a35b-88392aae7e13RxCUI 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

N476420006130 followed by a unit qualifier and the quantity

Package 76420-0061-30. 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 Aug 31, 2022.

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)

About NDC 76420-061

What is NDC 76420-061?: 76420-061 is the product NDC for Sildenafil, Sildenafil citrate 20 mg/1 tablet, film coated, listed with the FDA by Asclemed USA, Inc.. It has 3 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?: Asclemed USA, Inc., NDC labeler code 76420. 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
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Sildenafil	Sildenafil citrate 25 mg/1	Tablet, Film coatedOral	Jubilant Cadista Pharmaceuticals Inc.	59746-434	59746-0434-0359746-0434-0459746-0434-05+2 more
Sildenafil	Sildenafil citrate 50 mg/1	Tablet, Film coatedOral	Jubilant Cadista Pharmaceuticals Inc.	59746-435	59746-0435-0159746-0435-0359746-0435-04+3 more
Sildenafil	Sildenafil citrate 100 mg/1	Tablet, Film coatedOral	Jubilant Cadista Pharmaceuticals Inc.	59746-436	59746-0436-0159746-0436-0359746-0436-04+3 more
Sildenafil	Sildenafil citrate 20 mg/1	TabletOral	REMEDYREPACK INC.	70518-4596	70518-4596-00
Sildenafilsildenafil citrate	Sildenafil citrate 25 mg/1	FilmOral	Yaral Pharma Inc.	82347-0205	82347-0205-0482347-0205-0582347-0205-06
Sildenafilsildenafil citrate	Sildenafil citrate 50 mg/1	FilmOral	Yaral Pharma Inc.	82347-0210	82347-0210-0482347-0210-0582347-0210-06
Sildenafilsildenafil citrate	Sildenafil citrate 75 mg/1	FilmOral	Yaral Pharma Inc.	82347-0215	82347-0215-0482347-0215-0582347-0215-06
Sildenafilsildenafil citrate	Sildenafil citrate 100 mg/1	FilmOral	Yaral Pharma Inc.	82347-0220	82347-0220-0482347-0220-0582347-0220-06
Sildenafil	Sildenafil citrate 20 mg/1	Tablet, Film coatedOral	Golden State Medical Supply, Inc.	51407-987	51407-0987-90
Sildenafil	Sildenafil citrate 20 mg/1	TabletOral	AvKARE	42291-937	42291-0937-90

All 151 Sildenafil NDCs

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
Product	Strength	Form · route	Labeler	Product NDC
Sildenafil	Sildenafil citrate 20 mg/1	Tablet, Film coatedOral	NuCare Pharmaceuticals,Inc.	68071-5115
Sildenafil	Sildenafil citrate 20 mg/1	Tablet, Film coatedOral	NuCare Pharmaceuticals,Inc.	68071-4517
Sildenafil	Sildenafil citrate 20 mg/1	Tablet, Film coatedOral	Bryant Ranch Prepack	71335-1005
Sildenafil	Sildenafil citrate 20 mg/1	Tablet, Film coatedOral	BluePoint Laboratories	68001-597
Sildenafil	Sildenafil citrate 20 mg/1	Tablet, Film coatedOral	NuCare Pharmaceuticals, Inc.	68071-2072
Sildenafil	Sildenafil citrate 20 mg/1	Tablet, Film coatedOral	Proficient Rx LP	63187-813
Sildenafil	Sildenafil citrate 20 mg/1	Tablet, Film coatedOral	Macleods Pharmaceuticals Limited	33342-121
Sildenafil	Sildenafil citrate 20 mg/1	Tablet, Film coatedOral	American Health Packaging	60687-788
Sildenafil	Sildenafil citrate 20 mg/1	Tablet, Film coatedOral	BluePoint Laboratories	68001-363
Sildenafil	Sildenafil citrate 20 mg/1	Tablet, Film coatedOral	Macleods Pharmaceuticals Limited	33342-536
Sildenafil	Sildenafil citrate 20 mg/1	Tablet, Film coatedOral	Bryant Ranch Prepack	71335-1638