NDC codes

FDA NDC Directory
Product NDC (as listed)82804-185Labeler and product segments. Claims need a package NDC.
Product NDC at billing width82804-0185Add 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
82804-185-308280401853030 TABLET in 1 BOTTLE (82804-185-30)Marketed from Aug 6, 2025
82804-185-908280401859090 TABLET in 1 BOTTLE (82804-185-90)Marketed from Feb 6, 2025

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
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 210394
Marketing start
Listing expires
Other FDA classes
Phosphodiesterase 5 Inhibitors (Mechanism)
Identifiers
Product ID 82804-185_3c68969c-9034-4913-8ba1-5b0a43234eadSPL ID 3c68969c-9034-4913-8ba1-5b0a43234eadSPL set ID 7dd302cd-b84d-4d7d-bd1e-2916febbaea5RxCUI 577033UNII BW9B0ZE037UPC 0382804185900
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

N482804018530 followed by a unit qualifier and the quantity

Package 82804-0185-30. 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

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

Other NDCs under ANDA 210394

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

FDA NDC Directory listings under ANDA 210394
ProductStrengthForm · routeLabelerProduct NDC
SildenafilSildenafil citrate 20 mg/1TabletOralQuallent Pharmaceuticals Health LLC82009-094
SildenafilSildenafil citrate 20 mg/1TabletOralAjanta Pharma USA Inc.27241-124
SildenafilSildenafil citrate 20 mg/1TabletOralREMEDYREPACK INC.70518-3433
SildenafilSildenafil citrate 20 mg/1TabletOralBryant Ranch Prepack71335-1963
SildenafilSildenafil citrate 20 mg/1TabletOralDirectRx72189-298
SildenafilSildenafil citrate 20 mg/1TabletOralNuCare Pharmaceuticals,Inc.68071-2537
SildenafilSildenafil citrate 20 mg/1TabletOralNuCare Pharmaceuticals,Inc.68071-2602
SildenafilSildenafil citrate 20 mg/1TabletOralPreferred Pharmaceuticals Inc.68788-7974

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