NDC codes

FDA NDC Directory
Product NDC (as listed)70752-125Labeler and product segments. Claims need a package NDC.
Product NDC at billing width70752-0125Add 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
70752-125-1070752012510100 TABLET in 1 BOTTLE, PLASTIC (70752-125-10)Marketed from Aug 11, 2025
70752-125-11707520125111000 TABLET in 1 BOTTLE, PLASTIC (70752-125-11)Marketed from Aug 11, 2025

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 mesylate2 mg/1
Dosage form
Tablet
Route
Oral
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 70752-125_073409b4-0ae6-43d5-804a-a15ca581ecd9SPL ID 073409b4-0ae6-43d5-804a-a15ca581ecd9SPL set ID e1f0a249-e660-4592-9ffc-1c02b1022778RxCUI 885209, 885213, 885219UNII 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

N470752012510 followed by a unit qualifier and the quantity

Package 70752-0125-10. 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)

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 1 mg/1TabletOralBryant Ranch Prepack72162-2595
Benztropine MesylateBenztropine mesylate .5 mg/1TabletOralBryant Ranch Prepack72162-2594
Benztropine MesylateBenztropine mesylate 2 mg/1TabletOralBryant Ranch Prepack72162-2596
Benztropine MesylateBenztropine mesylate 1 mg/1TabletOralQUAGEN PHARMACEUTICALS LLC70752-124
Benztropine MesylateBenztropine mesylate .5 mg/1TabletOralQUAGEN PHARMACEUTICALS LLC70752-123

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