Prescription drug · ANDA
Trihexyphenidyl Hydrochloride NDC 63850-0021
Trihexyphenidyl hydrochloride 2 mg/1 · Tablet · Oral · Natco Pharma Limited
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 63850-0021-1 | 6385000210163850002101 | 100 TABLET in 1 BOTTLE (63850-0021-1)Marketed from Oct 17, 2010 | |
| 63850-0021-2 | 6385000210263850002102 | 250 TABLET in 1 BOTTLE (63850-0021-2)Marketed from Oct 17, 2010 | |
| 63850-0021-3 | 6385000210363850002103 | 1000 TABLET in 1 BOTTLE (63850-0021-3)Marketed from Oct 17, 2010 |
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)
- Trihexyphenidyl Hydrochloride
- Generic name (nonproprietary)
- trihexyphenidyl hydrochloride
- Active ingredients
- Trihexyphenidyl hydrochloride — 2 mg/1
- Dosage form
- Tablet
- Route
- Oral
- Labeler
- Natco Pharma LimitedNDC labeler code 63850
- Product type
- Prescription drug
- Marketing category
- ANDA — Abbreviated New Drug Application (generic)Application ANDA 091630
- Marketing start
- Listing expires
- Identifiers
- Product ID 63850-0021_2b77cfd6-ad8a-4cbf-a22c-eb69e7a8548cSPL ID 2b77cfd6-ad8a-4cbf-a22c-eb69e7a8548cSPL set ID b7e4200c-feff-4537-aad1-cf9989fd8c14RxCUI 905269, 905283UNII AO61G82577UPC 0363850002113, 0363850002229
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
N463850002101followed by a unit qualifier and the quantityPackage 63850-0021-01. 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 HCl 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.
About NDC 63850-0021
- What is NDC 63850-0021?
- 63850-0021 is the product NDC for Trihexyphenidyl Hydrochloride, Trihexyphenidyl hydrochloride 2 mg/1 tablet, listed with the FDA by Natco Pharma Limited. It has 3 package NDCs, 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?
- Natco Pharma Limited, NDC labeler code 63850. 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.
Related NDCs: other Trihexyphenidyl Hydrochloride products
Other finished products listed under the same name: strengths, forms and labelers.
| Product | Strength | Form · route | Labeler | Product NDC | Package NDCs (11-digit) |
|---|---|---|---|---|---|
| Trihexyphenidyl Hydrochloride | Trihexyphenidyl hydrochloride 5 mg/1 | TabletOral | REMEDYREPACK INC. | 70518-2409 | 70518-2409-02 |
| Trihexyphenidyl Hydrochloride | Trihexyphenidyl hydrochloride 2 mg/1 | TabletOral | REMEDYREPACK INC. | 70518-2410 | 70518-2410-05 |
| Trihexyphenidyl Hydrochloride | Trihexyphenidyl hydrochloride 5 mg/1 | TabletOral | Novitium Pharma LLC | 70954-211 | 70954-0211-1070954-0211-20 |
| Trihexyphenidyl Hydrochloride | Trihexyphenidyl hydrochloride 2 mg/1 | TabletOral | Novitium Pharma LLC | 70954-212 | 70954-0212-1070954-0212-20 |
| Trihexyphenidyl Hydrochloride | Trihexyphenidyl hydrochloride 5 mg/1 | TabletOral | REMEDYREPACK INC. | 70518-1657 | 70518-1657-01 |
| Trihexyphenidyl Hydrochloride | Trihexyphenidyl hydrochloride 2 mg/1 | TabletOral | REMEDYREPACK INC. | 70518-1612 | 70518-1612-01 |
| Trihexyphenidyl Hydrochloride | Trihexyphenidyl hydrochloride 5 mg/1 | TabletOral | REMEDYREPACK INC. | 70518-1140 | 70518-1140-00 |
| Trihexyphenidyl Hydrochloride | Trihexyphenidyl hydrochloride 5 mg/1 | TabletOral | Natco Pharma Limited | 63850-0022 | 63850-0022-0163850-0022-02 |
| Trihexyphenidyl Hydrochloride | Trihexyphenidyl hydrochloride 2 mg/5mL | SyrupOral | Akorn | 61748-054 | 61748-0054-16 |
| Trihexyphenidyl Hydrochloride | Trihexyphenidyl hydrochloride 2 mg/5mL | SolutionOral | Chartwell RX, LLC | 62135-065 | 62135-0065-47 |
Other NDCs under ANDA 091630
Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.
| Product | Strength | Form · route | Labeler | Product NDC |
|---|---|---|---|---|
| Trihexyphenidyl Hydrochloride | Trihexyphenidyl hydrochloride 5 mg/1 | TabletOral | Natco Pharma Limited | 63850-0022 |