NDC codes

FDA NDC Directory
Product NDC (as listed)46708-193Labeler and product segments. Claims need a package NDC.
Product NDC at billing width46708-0193Add 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
46708-193-08467080193084670801930880 TABLET, COATED in 1 CARTON (46708-193-08)Marketed from May 20, 2019
46708-193-30467080193304670801933030 TABLET, COATED in 1 BOTTLE (46708-193-30)Marketed from May 20, 2019
46708-193-90467080193904670801939090 TABLET, COATED in 1 BOTTLE (46708-193-90)Marketed from May 20, 2019
46708-193-9146708019391467080193911000 TABLET, COATED in 1 BOTTLE (46708-193-91)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 — 10 mg/1
Dosage form
Tablet, Coated
Route
Oral
Labeler
Alembic Pharmaceuticals LimitedNDC labeler code 46708
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 205575
Marketing start
Listing expires
Other FDA classes
Cholinergic Muscarinic Antagonists (Mechanism)
Identifiers
Product ID 46708-193_aea71cde-6d62-4f8d-b813-47064cb213d9SPL ID aea71cde-6d62-4f8d-b813-47064cb213d9SPL set ID aea71cde-6d62-4f8d-b813-47064cb213d9RxCUI 477367, 477372UNII KKA5DLD701UPC 0346708193300
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

N446708019308 followed by a unit qualifier and the quantity

Package 46708-0193-08. 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 tablet is a muscarinic antagonist indicated for the treatment of overactive bladder with symptoms of urge urinary incontinence, urgency, and urinary frequency. Solifenacin succinate tablets are muscarinic antagonist indicated for the treatment of 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)

About NDC 46708-193

What is NDC 46708-193?
46708-193 is the product NDC for Solifenacin Succinate, Solifenacin succinate 10 mg/1 tablet, coated, listed with the FDA by Alembic Pharmaceuticals Limited. It has 4 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Solifenacin Succinate.
What is the active ingredient?
Solifenacin succinate.
Who is the labeler?
Alembic Pharmaceuticals Limited, NDC labeler code 46708. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Solifenacin Succinate?
50 other product NDCs are listed under this name. See all Solifenacin Succinate NDCs.
Is there a related HCPCS / J-code?
Not in Med-Code's curated HCPCS directory. See Billing references above.

Other finished products listed under the same name: strengths, forms and labelers.

Other Solifenacin Succinate NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Solifenacin succinateSolifenacin succinate 5 mg/1Tablet, Film coatedOralHEC Pharm USA Inc.72303-083172303-0831-0172303-0831-02
Solifenacin succinateSolifenacin succinate 10 mg/1Tablet, Film coatedOralHEC Pharm USA Inc.72303-083272303-0832-0172303-0832-02
solifenacin succinateSolifenacin succinate 5 mg/1Tablet, CoatedOralMacleods Pharmaceuticals Limited33342-14833342-0148-0733342-0148-10
solifenacin succinateSolifenacin succinate 10 mg/1Tablet, CoatedOralMacleods Pharmaceuticals Limited33342-14933342-0149-0733342-0149-10
Solifenacin SuccinateSolifenacin succinate 5 mg/1Tablet, Film coatedOralAurobindo Pharma Limited65862-87865862-0878-0365862-0878-3065862-0878-90+1 more
Solifenacin SuccinateSolifenacin succinate 10 mg/1Tablet, Film coatedOralAurobindo Pharma Limited65862-87965862-0879-0365862-0879-3065862-0879-90+1 more
solifenacin succinateSolifenacin succinate 5 mg/1Tablet, Film coatedOralCamber Pharmaceuticals, Inc.31722-02731722-0027-3031722-0027-3131722-0027-90
solifenacin succinateSolifenacin succinate 10 mg/1Tablet, Film coatedOralCamber Pharmaceuticals, Inc.31722-02831722-0028-3031722-0028-3131722-0028-90
Solifenacin Succinatesolifenacin succiateSolifenacin succinate 5 mg/1Tablet, Film coatedOralAvKARE42291-73942291-0739-3042291-0739-90
Solifenacin SuccinateSolifenacin succinate 10 mg/1Tablet, Film coatedOralAvKARE42291-74042291-0740-3042291-0740-90

All 51 Solifenacin Succinate NDCs

Other NDCs under ANDA 205575

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

FDA NDC Directory listings under ANDA 205575
ProductStrengthForm · routeLabelerProduct NDC
Solifenacin SuccinateSolifenacin succinate 5 mg/1Tablet, CoatedOralAlembic Pharmaceuticals Limited46708-192
Solifenacin SuccinateSolifenacin succinate 5 mg/1Tablet, CoatedOralAlembic Pharmaceuticals Inc.62332-192
Solifenacin SuccinateSolifenacin succinate 10 mg/1Tablet, CoatedOralAlembic Pharmaceuticals Inc.62332-193

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