NDC codes

FDA NDC Directory
Product NDC (as listed)50228-427Labeler and product segments. Claims need a package NDC.
Product NDC at billing width50228-0427Add 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
50228-427-0550228042705500 TABLET, FILM COATED in 1 BOTTLE (50228-427-05)Marketed from May 20, 2019
50228-427-305022804273030 TABLET, FILM COATED in 1 BOTTLE (50228-427-30)Marketed from May 20, 2019
50228-427-905022804279090 TABLET, FILM COATED in 1 BOTTLE (50228-427-90)Marketed from May 20, 2019

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)
Solifenacin Succinate
Generic name (nonproprietary)
solifenacin succinate
Active ingredients
Solifenacin succinate — 5 mg/1
Dosage form
Tablet, Film coated
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 211657
Marketing start
Listing expires
Other FDA classes
Cholinergic Muscarinic Antagonists (Mechanism)
Identifiers
Product ID 50228-427_b9432117-2521-7360-e053-2a95a90acd2aSPL ID b9432117-2521-7360-e053-2a95a90acd2aSPL set ID a6f154d9-7463-4b80-b80e-c06a06e36141RxCUI 477367, 477372UNII KKA5DLD701UPC 0350228428903, 0350228428057, 0350228428309, 0350228427050, 0350228427906, 0350228427302
Pharmacologic class
Cholinergic Muscarinic Antagonist

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

N450228042705 followed by a unit qualifier and the quantity

Package 50228-0427-05. 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)

Solifenacin succinate is indicated for the treatment of adults with overactive bladder with symptoms of urge urinary incontinence, urgency, and urinary frequency. Solifenacin succinate is a muscarinic antagonist indicated for the treatment of adults with overactive bladder with symptoms of urge urinary incontinence, urgency, and urinary frequency. ( 1 )

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 211657

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

FDA NDC Directory listings under ANDA 211657
ProductStrengthForm · routeLabelerProduct NDC
Solifenacin SuccinateSolifenacin succinate 5 mg/1Tablet, Film coatedOralBryant Ranch Prepack63629-8532
Solifenacin SuccinateSolifenacin succinate 5 mg/1Tablet, Film coatedOralBryant Ranch Prepack71335-2423
Solifenacin SuccinateSolifenacin succinate 10 mg/1Tablet, Film coatedOralScieGen Pharmaceuticals, Inc.50228-428
Solifenacin SuccinateSolifenacin succinate 5 mg/1Tablet, Film coatedOralGolden State Medical Supply, Inc.51407-471
Solifenacin SuccinateSolifenacin succinate 10 mg/1Tablet, Film coatedOralGolden State Medical Supply, Inc.51407-472

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