NDC codes

FDA NDC Directory
Product NDC (as listed)82804-266Labeler and product segments. Claims need a package NDC.
Product NDC at billing width82804-0266Add 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
82804-266-308280402663030 TABLET, FILM COATED in 1 BOTTLE (82804-266-30)Marketed from Feb 5, 2026

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 — 10 mg/1
Dosage form
Tablet, Film coated
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 211701
Marketing start
Listing expires
Other FDA classes
Cholinergic Muscarinic Antagonists (Mechanism)
Identifiers
Product ID 82804-266_1d8e8f6f-0a59-479f-8415-c5c5f19e1977SPL ID 1d8e8f6f-0a59-479f-8415-c5c5f19e1977SPL set ID 1d8e8f6f-0a59-479f-8415-c5c5f19e1977RxCUI 477372UNII KKA5DLD701UPC 0382804266302
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

N482804026630 followed by a unit qualifier and the quantity

Package 82804-0266-30. 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

Current FDA label (SPL), effective .

Indications (excerpt from the label)

Solifenacin succinate tablets are indicated for the treatment of adults with overactive bladder with symptoms of urge urinary incontinence, urgency, and urinary frequency. Solifenacin succinate tablets are 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 211701

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

FDA NDC Directory listings under ANDA 211701
ProductStrengthForm · routeLabelerProduct NDC
Solifenacin SuccinateSolifenacin succinate 5 mg/1Tablet, Film coatedOralProficient Rx LP82804-044
Solifenacin SuccinateSolifenacin succinate 5 mg/1Tablet, Film coatedOralUnichem Pharmaceuticals (USA), Inc.29300-328
Solifenacin SuccinateSolifenacin succinate 10 mg/1Tablet, Film coatedOralUnichem Pharmaceuticals (USA), Inc.29300-329

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