NDC codes

FDA NDC Directory
Product NDC (as listed)72789-324Labeler and product segments. Claims need a package NDC.
Product NDC at billing width72789-0324Add 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
72789-324-907278903249090 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-324-90)Marketed from May 24, 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)
tadalafil
Generic name (nonproprietary)
tadalafil
Active ingredients
Tadalafil — 5 mg/1
Dosage form
Tablet, Film coated
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 215556
Marketing start
Listing expires
Other FDA classes
Phosphodiesterase 5 Inhibitors (Mechanism)
Identifiers
Product ID 72789-324_40bb2f8b-c4c1-4ec3-e063-6394a90ae8dcSPL ID 40bb2f8b-c4c1-4ec3-e063-6394a90ae8dcSPL set ID fc7596dd-42d3-af7c-e053-6294a90af01eRxCUI 403957UNII 742SXX0ICTUPC 0372789324906
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

N472789032490 followed by a unit qualifier and the quantity

Package 72789-0324-90. 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)

Tadalafil is a phosphodiesterase 5 (PDE5) inhibitor indicated for the treatment of: erectile dysfunction (ED) ( 1.1 ) the signs and symptoms of benign prostatic hyperplasia (BPH) ( 1.2 ) ED and the signs and symptoms of BPH (ED/BPH) ( 1.3 ) If tadalafil is used with finasteride to initiate BPH treatment, such use is recommended for up to 26 weeks ( 1.4 ). 1.1 Erectile Dysfunction Tadalafil tablets are indicated for the treatment of erectile dysfunction (ED). 1.2 Benign Prostatic Hyperplasia Tadalafil tablets are indicated for the treatment of the signs and symptoms of benign prostatic hyperplasia (BPH). 1.3 Erectile Dysfunction and Benign Prostatic Hyperplasia Tadalafil tablets are indicated…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 215556

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

FDA NDC Directory listings under ANDA 215556
ProductStrengthForm · routeLabelerProduct NDC
tadalafilTadalafil 10 mg/1Tablet, Film coatedOralPD-Rx Pharmaceuticals, Inc.72789-430
tadalafilTadalafil 5 mg/1Tablet, Film coatedOralBurel Pharmaceuticals, LLC35573-461
tadalafilTadalafil 2.5 mg/1Tablet, Film coatedOralBurel Pharmaceuticals, LLC35573-460
tadalafilTadalafil 10 mg/1Tablet, Film coatedOralBurel Pharmaceuticals, LLC35573-462
tadalafilTadalafil 20 mg/1Tablet, Film coatedOralBurel Pharmaceuticals, LLC35573-463
tadalafilTadalafil 5 mg/1Tablet, Film coatedOralA-S Medication Solutions50090-7314
tadalafilTadalafil 5 mg/1Tablet, Film coatedOralA-S Medication Solutions50090-7315
tadalafilTadalafil 20 mg/1Tablet, Film coatedOralVKT Pharma Private Limited71821-009
tadalafilTadalafil 2.5 mg/1Tablet, Film coatedOralVKT Pharma Private Limited71821-006
tadalafilTadalafil 5 mg/1Tablet, Film coatedOralVKT Pharma Private Limited71821-007
tadalafilTadalafil 10 mg/1Tablet, Film coatedOralVKT Pharma Private Limited71821-008
tadalafilTadalafil 20 mg/1Tablet, Film coatedOralPD-Rx Pharmaceuticals, Inc.72789-344

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