Sildenafil NDC 50090-7977

NDC codes

FDA NDC Directory

Product NDC (as listed)50090-7977Labeler and product segments. Claims need a package NDC.

Product NDC at billing width50090-7977Add 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	Copy
50090-7977-0	50090797700	10 TABLET, FILM COATED in 1 BOTTLE (50090-7977-0)Marketed from May 18, 2026

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 — 50 mg/1
Dosage form: Tablet, Film coated
Route: Oral
Labeler: A-S Medication Solutions
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 202255
Marketing start: Apr 19, 2023
Listing expires: Dec 31, 2027
Other FDA classes: Phosphodiesterase 5 Inhibitors (Mechanism)
Identifiers: Product ID 50090-7977_9cf5bf4b-5c76-44ef-9712-c7ad981203efSPL ID 9cf5bf4b-5c76-44ef-9712-c7ad981203efSPL set ID 9143e0ab-0fa1-4718-919c-ddfd1e9b8386RxCUI 312950UNII 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

N450090797700 followed by a unit qualifier and the quantity

Package 50090-7977-00. 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

Label details couldn’t be retrieved right now. Open the label on DailyMed.

Other NDCs under ANDA 202255

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

FDA NDC Directory listings under ANDA 202255
Product	Strength	Form · route	Labeler	Product NDC
Sildenafil	Sildenafil citrate 50 mg/1	Tablet, Film coatedOral	Macleods Pharmaceuticals Limited	33342-042
Sildenafil	Sildenafil citrate 25 mg/1	Tablet, Film coatedOral	Macleods Pharmaceuticals Limited	33342-041
Sildenafil	Sildenafil citrate 100 mg/1	Tablet, Film coatedOral	Macleods Pharmaceuticals Limited	33342-043
Sildenafil	Sildenafil citrate 50 mg/1	Tablet, Film coatedOral	NuCare Pharmaceuticals, Inc.	68071-3978