NDC codes

FDA NDC Directory
Product NDC (as listed)72162-2595Labeler and product segments. Claims need a package NDC.
Product NDC at billing width72162-2595Add 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
72162-2595-072162259500721622595001000 TABLET in 1 BOTTLE (72162-2595-0)Marketed from Jan 7, 2026
72162-2595-17216225950172162259501100 TABLET in 1 BOTTLE (72162-2595-1)Marketed from Jan 7, 2026
72162-2595-27216225950272162259502100 TABLET in 1 BOTTLE, PLASTIC (72162-2595-2)Marketed from Jan 7, 2026

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)
Benztropine Mesylate
Generic name (nonproprietary)
benztropine mesylate
Active ingredients
Benztropine mesylate — 1 mg/1
Dosage form
Tablet
Route
Oral
Labeler
Bryant Ranch PrepackNDC labeler code 72162
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 212694
Marketing start
Listing expires
Other FDA classes
Cholinergic Antagonists (Mechanism)Histamine Receptor Antagonists (Mechanism)
Identifiers
Product ID 72162-2595_36677fd5-dd41-445d-b912-49904af6ce6dSPL ID 36677fd5-dd41-445d-b912-49904af6ce6dSPL set ID 9270d14c-b885-4679-8871-6f2547450398RxCUI 885213UNII WMJ8TL7510
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

N472162259500 followed by a unit qualifier and the quantity

Package 72162-2595-00. 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 Benztropine mesylate tablets are indicated 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 72162-2595

What is NDC 72162-2595?
72162-2595 is the product NDC for Benztropine Mesylate, Benztropine mesylate 1 mg/1 tablet, listed with the FDA by Bryant Ranch Prepack. It has 3 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?
Bryant Ranch Prepack, NDC labeler code 72162. 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 212694

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

FDA NDC Directory listings under ANDA 212694
ProductStrengthForm · routeLabelerProduct NDC
Benztropine MesylateBenztropine mesylate .5 mg/1TabletOralQUAGEN PHARMACEUTICALS LLC70752-123
Benztropine MesylateBenztropine mesylate 1 mg/1TabletOralQUAGEN PHARMACEUTICALS LLC70752-124
Benztropine MesylateBenztropine mesylate 2 mg/1TabletOralQUAGEN PHARMACEUTICALS LLC70752-125
Benztropine MesylateBenztropine mesylate .5 mg/1TabletOralBryant Ranch Prepack72162-2594
Benztropine MesylateBenztropine mesylate 2 mg/1TabletOralBryant Ranch Prepack72162-2596

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