NDC codes

FDA NDC Directory
Product NDC (as listed)70518-0577Labeler and product segments. Claims need a package NDC.
Product NDC at billing width70518-0577Add 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
70518-0577-0705180577007051805770030 TABLET in 1 BLISTER PACK (70518-0577-0)Marketed from Jun 19, 2017
70518-0577-2705180577027051805770230 TABLET in 1 BLISTER PACK (70518-0577-2)Marketed from Jun 9, 2020
70518-0577-57051805770570518057705100 POUCH in 1 BOX (70518-0577-5) / 1 TABLET in 1 POUCH (70518-0577-6)Marketed from Jan 23, 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
REMEDYREPACK INC.NDC labeler code 70518
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 090168
Marketing start
Listing expires
Other FDA classes
Cholinergic Antagonists (Mechanism)Histamine Receptor Antagonists (Mechanism)
Identifiers
Product ID 70518-0577_5563ab2e-709a-1c8f-e063-6294a90a8503SPL ID 5563ab2e-709a-1c8f-e063-6294a90a8503SPL set ID 01688e6f-7b22-41bf-9a85-1c88d90f99b6RxCUI 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

N470518057700 followed by a unit qualifier and the quantity

Package 70518-0577-00. 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, USP 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 70518-0577

What is NDC 70518-0577?
70518-0577 is the product NDC for Benztropine Mesylate, Benztropine mesylate 1 mg/1 tablet, listed with the FDA by REMEDYREPACK INC.. 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?
REMEDYREPACK INC., NDC labeler code 70518. 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 090168

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

FDA NDC Directory listings under ANDA 090168
ProductStrengthForm · routeLabelerProduct NDC
Benztropine MesylateBenztropine mesylate 1 mg/1TabletOralProficient Rx LP63187-840
Benztropine MesylateBenztropine mesylate .5 mg/1TabletOralLeading Pharma, LLC69315-136
Benztropine MesylateBenztropine mesylate 1 mg/1TabletOralLeading Pharma, LLC69315-137
Benztropine MesylateBenztropine mesylate 2 mg/1TabletOralLeading Pharma, LLC69315-138
Benztropine MesylateBenztropine mesylate 2 mg/1TabletOralREMEDYREPACK INC.70518-2677
Benztropine MesylateBenztropine mesylate .5 mg/1TabletOralREMEDYREPACK INC.70518-2732
Benztropine MesylateBenztropine mesylate 1 mg/1TabletOralAphena Pharma Solutions - Tennessee, LLC71610-502

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