NDC codes

FDA NDC Directory
Product NDC (as listed)11534-169Labeler and product segments. Claims need a package NDC.
Product NDC at billing width11534-0169Add 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
11534-169-091153401690911534016909100 TABLET in 1 BOTTLE (11534-169-09)Marketed from Oct 16, 2024
11534-169-1011534016910115340169101000 TABLET in 1 BOTTLE (11534-169-10)Marketed from Oct 16, 2024

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)
Benztropine Mesylate
Generic name (nonproprietary)
benztropine mesylate
Active ingredients
Benztropine mesylate — 2 mg/1
Dosage form
Tablet
Route
Oral
Labeler
SUNRISE PHARMACEUTICAL, INCNDC labeler code 11534
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 204713
Marketing start
Listing expires
Other FDA classes
Cholinergic Antagonists (Mechanism)Histamine Receptor Antagonists (Mechanism)
Identifiers
Product ID 11534-169_192d20d2-c01e-4150-beb0-03f8da966accSPL ID 192d20d2-c01e-4150-beb0-03f8da966accSPL set ID 2c988462-ce77-4e99-b98e-8f6ad519e295RxCUI 885209, 885213, 885219UNII WMJ8TL7510UPC 0311534168099, 0311534168105, 0311534169096, 0311534169102, 0311534167108, 0311534167092
Pharmacologic class
Anticholinergic; Antihistamine

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

N411534016909 followed by a unit qualifier and the quantity

Package 11534-0169-09. 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)

INDICATIONS AND USAGE For use as an adjunct in the therapy of all forms of parkinsonism. Useful also in the control of extrapyramidal disorders (except tardive dyskinesia - see PRECAUTIONS ) due to neuroleptic drugs (e.g., phenothiazines).

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 11534-169

What is NDC 11534-169?
11534-169 is the product NDC for Benztropine Mesylate, Benztropine mesylate 2 mg/1 tablet, listed with the FDA by SUNRISE PHARMACEUTICAL, INC. It has 2 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Benztropine Mesylate.
What is the active ingredient?
Benztropine mesylate.
Who is the labeler?
SUNRISE PHARMACEUTICAL, INC, NDC labeler code 11534. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Benztropine Mesylate?
55 other product NDCs are listed under this name. See all Benztropine Mesylate 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 Benztropine Mesylate NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Benztropine MesylateBenztropine mesylate 1 mg/1TabletOralUnit Dose Solutions, Inc.87441-01287441-0012-01
Benztropine MesylateBenztropine mesylate 2 mg/1TabletOralCoupler LLC67046-004067046-0040-03
Benztropine MesylateBenztropine mesylate 2 mg/1TabletOralCoupler LLC67046-167567046-1675-03
Benztropine MesylateBenztropine mesylate .5 mg/1TabletOralCoupler LLC67046-120567046-1205-03
Benztropine MesylateBenztropine mesylate .5 mg/1TabletOralCoupler LLC67046-167467046-1674-03
Benztropine MesylateBenztropine mesylate 1 mg/1TabletOralCoupler LLC67046-004167046-0041-03
Benztropine MesylateBenztropine mesylate .5 mg/1TabletOralQUAGEN PHARMACEUTICALS LLC70752-12370752-0123-1070752-0123-11
Benztropine MesylateBenztropine mesylate 1 mg/1TabletOralQUAGEN PHARMACEUTICALS LLC70752-12470752-0124-1070752-0124-11
Benztropine MesylateBenztropine mesylate 2 mg/1TabletOralQUAGEN PHARMACEUTICALS LLC70752-12570752-0125-1070752-0125-11
Benztropine MesylateBenztropine mesylate .5 mg/1TabletOralBryant Ranch Prepack72162-259472162-2594-0072162-2594-0172162-2594-02

All 56 Benztropine Mesylate NDCs

Other NDCs under ANDA 204713

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

FDA NDC Directory listings under ANDA 204713
ProductStrengthForm · routeLabelerProduct NDC
Benztropine MesylateBenztropine mesylate .5 mg/1TabletOralMarlex PHARMACEUTICAL, INC10135-813
Benztropine MesylateBenztropine mesylate 1 mg/1TabletOralMarlex PHARMACEUTICAL, INC10135-814
Benztropine MesylateBenztropine mesylate 2 mg/1TabletOralMarlex PHARMACEUTICAL, INC10135-815
Benztropine MesylateBenztropine mesylate .5 mg/1TabletOralSUNRISE PHARMACEUTICAL, INC11534-167
Benztropine MesylateBenztropine mesylate 1 mg/1TabletOralSUNRISE PHARMACEUTICAL, INC11534-168

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