What is NDC 60290-079?

60290-079 is the product NDC for Sildenafil Citrate, Sildenafil citrate 25 mg/1 tablet, film coated, listed with the FDA by Umedica Laboratories USA Inc.. It has 4 package NDCs, shown above in 10- and 11-digit form.

Umedica Laboratories USA Inc., NDC labeler code 60290. 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 Citrate?

70 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Sildenafil Citrate NDC 60290-079 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)60290-079Labeler and product segments. Claims need a package NDC.

Product NDC at billing width60290-0079Add 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
60290-079-01	6029000790160290007901	30 TABLET, FILM COATED in 1 BOTTLE (60290-079-01)Marketed from Feb 15, 2026
60290-079-02	6029000790260290007902	90 TABLET, FILM COATED in 1 BOTTLE (60290-079-02)Marketed from Feb 15, 2026
60290-079-03	6029000790360290007903	1000 TABLET, FILM COATED in 1 BOTTLE (60290-079-03)Marketed from Feb 15, 2026
60290-079-04	6029000790460290007904	500 TABLET, FILM COATED in 1 BOTTLE (60290-079-04)Marketed from Apr 27, 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 Citrate
Generic name (nonproprietary): sildenafil citrate
Active ingredients: Sildenafil citrate — 25 mg/1
Dosage form: Tablet, Film coated
Route: Oral
Labeler: Umedica Laboratories USA Inc.NDC labeler code 60290
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 209302
Marketing start: Feb 15, 2026
Listing expires: Dec 31, 2027
Other FDA classes: Phosphodiesterase 5 Inhibitors (Mechanism)
Identifiers: Product ID 60290-079_51b76a30-43fd-eaa4-e063-6394a90a286dSPL ID 51b76a30-43fd-eaa4-e063-6394a90a286dSPL set ID 90477a51-63ba-43f4-a74b-4659a946093cRxCUI 312950, 314228, 314229UNII BW9B0ZE037UPC 0360290003021, 0360290003014, 0360290079033, 0360290002031, 0360290002017, 0360290003038
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

N460290007901 followed by a unit qualifier and the quantity

Package 60290-0079-01. 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 Oct 23, 2026.

Indications (excerpt from the label)

Sildenafil tablets are indicated for the treatment of erectile dysfunction. Sildenafil is a phosphodiesterase-5 (PDE5) inhibitor indicated for the treatment of erectile dysfunction (ED)

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 60290-079

What is NDC 60290-079?: 60290-079 is the product NDC for Sildenafil Citrate, Sildenafil citrate 25 mg/1 tablet, film coated, listed with the FDA by Umedica Laboratories USA Inc.. It has 4 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Sildenafil Citrate.
What is the active ingredient?: Sildenafil citrate.
Who is the labeler?: Umedica Laboratories USA Inc., NDC labeler code 60290. 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 Citrate?: 70 other product NDCs are listed under this name. See all Sildenafil Citrate 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 Citrate NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Sildenafil Citratesildenafil	Sildenafil citrate 100 mg/1	Tablet, Film coatedOral	Preferred Pharmaceuticals Inc.	68788-4111	68788-4111-0168788-4111-0368788-4111-07
Sildenafil Citrate	Sildenafil citrate 100 mg/1	TabletOral	Aphena Pharma Solutions - Tennessee, LLC	53401-046	53401-0046-52
Sildenafil Citrate	Sildenafil citrate 25 mg/1	TabletOral	Northstar Rx LLC	72603-883	72603-0883-01
Sildenafil Citrate	Sildenafil citrate 50 mg/1	TabletOral	Northstar Rx LLC	72603-884	72603-0884-01
Sildenafil Citrate	Sildenafil citrate 100 mg/1	TabletOral	Northstar Rx LLC	72603-885	72603-0885-0172603-0885-02
Sildenafil Citrate	Sildenafil citrate 50 mg/1	Tablet, Film coatedOral	Umedica Laboratories USA Inc.	60290-002	60290-0002-0160290-0002-0260290-0002-03+1 more
Sildenafil Citrate	Sildenafil citrate 100 mg/1	Tablet, Film coatedOral	Umedica Laboratories USA Inc.	60290-003	60290-0003-0160290-0003-0260290-0003-03+2 more
Sildenafil Citratesildenafil	Sildenafil citrate 20 mg/1	Tablet, Film coatedOral	Northwind Health Company, LLC	82868-094	82868-0094-30
Sildenafil Citrate	Sildenafil citrate 100 mg/1	TabletOral	Advanced Rx of Tennessee, LLC	80425-0503	80425-0503-0180425-0503-0280425-0503-03
Sildenafil Citrate	Sildenafil citrate 100 mg/1	TabletOral	Preferred Pharmaceuticals Inc.	68788-8804	68788-8804-0168788-8804-0368788-8804-07

All 71 Sildenafil Citrate NDCs

Other NDCs under ANDA 209302

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

FDA NDC Directory listings under ANDA 209302
Product	Strength	Form · route	Labeler	Product NDC
Sildenafil Citrate	Sildenafil citrate 50 mg/1	TabletOral	A-S Medication Solutions	50090-7181
Sildenafil Citrate	Sildenafil citrate 50 mg/1	Tablet, Film coatedOral	Umedica Laboratories USA Inc.	60290-002
Sildenafil Citrate	Sildenafil citrate 100 mg/1	Tablet, Film coatedOral	Umedica Laboratories USA Inc.	60290-003
Sildenafil Citrate	Sildenafil citrate 100 mg/1	TabletOral	Preferred Pharmaceuticals Inc.	68788-8804
Sildenafil Citrate	Sildenafil citrate 100 mg/1	TabletOral	Proficient Rx LP	71205-657
Sildenafil Citrate	Sildenafil citrate 50 mg/1	TabletOral	Proficient Rx LP	71205-721
Sildenafil Citrate	Sildenafil citrate 50 mg/1	TabletOral	Proficient Rx LP	71205-795
Sildenafil Citrate	Sildenafil citrate 25 mg/1	TabletOral	Northstar Rx LLC	72603-883
Sildenafil Citrate	Sildenafil citrate 50 mg/1	TabletOral	Northstar Rx LLC	72603-884
Sildenafil Citrate	Sildenafil citrate 100 mg/1	TabletOral	Northstar Rx LLC	72603-885
Sildenafil Citrate	Sildenafil citrate 25 mg/1	TabletOral	PD-Rx Pharmaceuticals, Inc.	72789-404
Sildenafil Citrate	Sildenafil citrate 50 mg/1	TabletOral	PD-Rx Pharmaceuticals, Inc.	72789-405
Sildenafil Citrate	Sildenafil citrate 100 mg/1	TabletOral	PD-Rx Pharmaceuticals, Inc.	72789-406
Sildenafil Citrate	Sildenafil citrate 50 mg/1	TabletOral	NIVAGEN PHARMACEUTICALS, INC.	75834-240
Sildenafil Citrate	Sildenafil citrate 100 mg/1	TabletOral	NIVAGEN PHARMACEUTICALS, INC.	75834-241
Sildenafil Citrate	Sildenafil citrate 25 mg/1	TabletOral	NIVAGEN PHARMACEUTICALS, INC.	75834-272
Sildenafil Citrate	Sildenafil citrate 100 mg/1	TabletOral	Advanced Rx of Tennessee, LLC	80425-0503
Sildenafil Citrate	Sildenafil citrate 25 mg/1	TabletOral	Proficient Rx LP	82804-251