Sildenafil Citrate (sildenafil) NDC 68788-4111

Product information

Brand name (proprietary)

Sildenafil Citrate

Generic name (nonproprietary)

sildenafil

Active ingredients

Sildenafil citrate — 100 mg/1

Dosage form

Tablet, Film coated

Route

Oral

Labeler

Preferred Pharmaceuticals Inc.

Product type

Prescription drug

Marketing category

ANDA — Abbreviated New Drug Application (generic)Application ANDA 091448

Marketing start

Apr 22, 2026

Listing expires

Dec 31, 2027

Other FDA classes

Phosphodiesterase 5 Inhibitors (Mechanism)

Identifiers

Product ID 68788-4111_5f9ff0bb-5634-437a-96eb-249b910c7e81SPL ID 5f9ff0bb-5634-437a-96eb-249b910c7e81SPL set ID 5f9ff0bb-5634-437a-96eb-249b910c7e81RxCUI 314229UNII 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

N468788411101 followed by a unit qualifier and the quantity Copy

Package 68788-4111-01. 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

Other NDCs under ANDA 091448

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