NDC codes

FDA NDC Directory
Product NDC (as listed)62135-065Labeler and product segments. Claims need a package NDC.
Product NDC at billing width62135-0065Add 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
62135-065-476213500654762135006547473 mL in 1 BOTTLE (62135-065-47)Marketed from Jul 1, 2026

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)
Trihexyphenidyl Hydrochloride
Generic name (nonproprietary)
trihexyphenidyl hydrochloride
Active ingredients
Trihexyphenidyl hydrochloride — 2 mg/5mL
Dosage form
Solution
Route
Oral
Labeler
Chartwell RX, LLCNDC labeler code 62135
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 040251
Marketing start
Listing expires
Identifiers
Product ID 62135-065_56d1a3b3-bb71-903b-e063-6394a90a99fcSPL ID 56d1a3b3-bb71-903b-e063-6394a90a99fcSPL set ID e8e2ac3b-80dc-4449-9365-2586d6d57e10RxCUI 905273UNII AO61G82577UPC 0362135065478

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

N462135006547 followed by a unit qualifier and the quantity

Package 62135-0065-47. 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 Trihexyphenidyl is indicated as an adjunct in the treatment of all forms of parkinsonism (postencephalitic, arteriosclerotic, and idiopathic). It is often useful as adjuvant therapy when treating these forms of parkinsonism with levodopa. Additionally, it is indicated for the control of extrapyramidal disorders caused by central nervous system drugs such as the dibenzoxazepines, phenothiazines, thioxanthenes, and butyrophenones.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 62135-065

What is NDC 62135-065?
62135-065 is the product NDC for Trihexyphenidyl Hydrochloride, Trihexyphenidyl hydrochloride 2 mg/5mL solution, listed with the FDA by Chartwell RX, LLC. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Trihexyphenidyl Hydrochloride.
What is the active ingredient?
Trihexyphenidyl hydrochloride.
Who is the labeler?
Chartwell RX, LLC, NDC labeler code 62135. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Trihexyphenidyl Hydrochloride?
13 other product NDCs are listed under this name. See all Trihexyphenidyl Hydrochloride 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 Trihexyphenidyl Hydrochloride NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Trihexyphenidyl HydrochlorideTrihexyphenidyl hydrochloride 5 mg/1TabletOralREMEDYREPACK INC.70518-240970518-2409-02
Trihexyphenidyl HydrochlorideTrihexyphenidyl hydrochloride 2 mg/1TabletOralREMEDYREPACK INC.70518-241070518-2410-05
Trihexyphenidyl HydrochlorideTrihexyphenidyl hydrochloride 5 mg/1TabletOralNovitium Pharma LLC70954-21170954-0211-1070954-0211-20
Trihexyphenidyl HydrochlorideTrihexyphenidyl hydrochloride 2 mg/1TabletOralNovitium Pharma LLC70954-21270954-0212-1070954-0212-20
Trihexyphenidyl HydrochlorideTrihexyphenidyl hydrochloride 5 mg/1TabletOralREMEDYREPACK INC.70518-165770518-1657-01
Trihexyphenidyl HydrochlorideTrihexyphenidyl hydrochloride 2 mg/1TabletOralREMEDYREPACK INC.70518-161270518-1612-01
Trihexyphenidyl HydrochlorideTrihexyphenidyl hydrochloride 5 mg/1TabletOralREMEDYREPACK INC.70518-114070518-1140-00
Trihexyphenidyl HydrochlorideTrihexyphenidyl hydrochloride 2 mg/1TabletOralNatco Pharma Limited63850-002163850-0021-0163850-0021-0263850-0021-03
Trihexyphenidyl HydrochlorideTrihexyphenidyl hydrochloride 5 mg/1TabletOralNatco Pharma Limited63850-002263850-0022-0163850-0022-02
Trihexyphenidyl HydrochlorideTrihexyphenidyl hydrochloride 2 mg/5mLSyrupOralAkorn61748-05461748-0054-16

All 14 Trihexyphenidyl Hydrochloride NDCs

Other NDCs under ANDA 040251

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

FDA NDC Directory listings under ANDA 040251
ProductStrengthForm · routeLabelerProduct NDC
Trihexyphenidyl HydrochlorideTrihexyphenidyl hydrochloride 2 mg/5mLSyrupOralAkorn61748-054

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