NDC codes

FDA NDC Directory
Product NDC (as listed)60505-4702Labeler and product segments. Claims need a package NDC.
Product NDC at billing width60505-4702Add 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
60505-4702-36050547020330 TABLET, FILM COATED in 1 BOTTLE (60505-4702-3)Marketed from May 20, 2019

How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 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 209333
Marketing start
Marketing end
Other FDA classes
Cholinergic Muscarinic Antagonists (Mechanism)
Identifiers
Product ID 60505-4702_70d28c29-7862-4ead-a53f-d3646aba26ddSPL ID 70d28c29-7862-4ead-a53f-d3646aba26ddSPL set ID 1d96b386-febf-a510-a896-033e832c8f30RxCUI 477367, 477372UNII KKA5DLD701UPC 0360505470235, 0360505470334
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

N460505470203 followed by a unit qualifier and the quantity

Package 60505-4702-03. 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 209333

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

FDA NDC Directory listings under ANDA 209333
ProductStrengthForm · routeLabelerProduct NDC
Solifenacin SuccinateSolifenacin succinate 10 mg/1Tablet, Film coatedOralApotex Corp.60505-4703
Solifenacin SuccinateSolifenacin succinate 5 mg/1Tablet, Film coatedOralProficient Rx LP71205-559
Solifenacin Succinatesolifenacin succinate tabletsSolifenacin succinate 10 mg/1Tablet, Film coatedOralQilu Pharmaceutical Co., Ltd.67184-0517
Solifenacin SuccinateSolifenacin succinate 10 mg/1Tablet, Film coatedOralProficient Rx LP71205-583

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