NDC codes

FDA NDC Directory
Product NDC (as listed)70954-212Labeler and product segments. Claims need a package NDC.
Product NDC at billing width70954-0212Add 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
70954-212-1070954021210100 TABLET in 1 BOTTLE (70954-212-10)Marketed from Jan 28, 2019
70954-212-20709540212201000 TABLET in 1 BOTTLE (70954-212-20)Marketed from Jan 28, 2019

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 hydrochloride2 mg/1
Dosage form
Tablet
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 040254
Marketing start
Listing expires
Identifiers
Product ID 70954-212_83608c13-509d-448b-8559-5f5e8a9a0d75SPL ID 83608c13-509d-448b-8559-5f5e8a9a0d75SPL set ID 83608c13-509d-448b-8559-5f5e8a9a0d75RxCUI 905269, 905283UNII AO61G82577UPC 0370954212102, 0370954211105

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

N470954021210 followed by a unit qualifier and the quantity

Package 70954-0212-10. 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 & USAGE This drug 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)

Other NDCs under ANDA 040254

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

FDA NDC Directory listings under ANDA 040254
ProductStrengthForm · routeLabelerProduct NDC
Trihexyphenidyl HydrochlorideTrihexyphenidyl hydrochloride 5 mg/1TabletOralGolden State Medical Supply Inc.51407-266
Trihexyphenidyl HydrochlorideTrihexyphenidyl hydrochloride 2 mg/1TabletOralGolden State Medical Supply Inc.51407-265
Trihexyphenidyl HydrochlorideTrihexyphenidyl hydrochloride 5 mg/1TabletOralREMEDYREPACK INC.70518-2409
Trihexyphenidyl HydrochlorideTrihexyphenidyl hydrochloride 2 mg/1TabletOralREMEDYREPACK INC.70518-2410
Trihexyphenidyl HydrochlorideTrihexyphenidyl hydrochloride 5 mg/1TabletOralNovitium Pharma LLC70954-211

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