NDC codes

FDA NDC Directory
Product NDC (as listed)71209-106Labeler and product segments. Claims need a package NDC.
Product NDC at billing width71209-0106Add 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
71209-106-017120901060130 TABLET, FILM COATED in 1 BOTTLE (71209-106-01)Marketed from Dec 1, 2023
71209-106-0571209010605100 TABLET, FILM COATED in 1 BOTTLE (71209-106-05)Marketed from Dec 1, 2023
71209-106-11712090106111000 TABLET, FILM COATED in 1 BOTTLE (71209-106-11)Marketed from Dec 1, 2023

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 — 25 mg/1
Dosage form
Tablet, Film coated
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 218045
Marketing start
Listing expires
Other FDA classes
Phosphodiesterase 5 Inhibitors (Mechanism)
Identifiers
Product ID 71209-106_eff134c4-3240-4132-b9ea-118ce1fa719aSPL ID eff134c4-3240-4132-b9ea-118ce1fa719aSPL set ID c079fc41-7b9a-499d-88ea-86ccb65c828dRxCUI 312950, 314228, 314229UNII BW9B0ZE037UPC 0371209108010, 0377209102119, 0371209106054, 0371209107051, 0371209106016, 0371209107112, 0371209106115
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

N471209010601 followed by a unit qualifier and the quantity

Package 71209-0106-01. 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 .

Indications (excerpt from the label)

Sildenafil tablets are indicated for the treatment of erectile dysfunction. Sildenafil tablets are phosphodiesterase-5 (PDE5) inhibitor indicated for the treatment of erectile dysfunction (ED) (1)

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 218045

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

FDA NDC Directory listings under ANDA 218045
ProductStrengthForm · routeLabelerProduct NDC
SildenafilSildenafil citrate 100 mg/1Tablet, Film coatedOralCadila Pharmaceuticals Limited71209-108
SildenafilSildenafil citrate 50 mg/1Tablet, Film coatedOralCadila Pharmaceuticals Limited71209-107
SildenafilSildenafil citrate 100 mg/1Tablet, Film coatedOralModavar Pharmaceuticals LLC72241-071
SildenafilSildenafil citrate 25 mg/1Tablet, Film coatedOralModavar Pharmaceuticals LLC72241-069
SildenafilSildenafil citrate 50 mg/1Tablet, Film coatedOralModavar Pharmaceuticals LLC72241-070

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Sildenafil NDC 71209-106 | Med-Code