NDC 63850-0021-02 - Trihexyphenidyl Hydrochloride
This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.
- Product NDC
- 63850-0021
- Requested NDC
- 63850-0021-02
- Package NDCs from labels
- 63850-0021-1, 63850-0021-2, 63850-0021-3, 63850-0021-02
- Manufacturer
- Natco Pharma Limited | Natco Pharma Limited-Pharma Division
- Effective date
- 2019-10-25
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| TRIHEXYPHENIDYL - Natco Pharma Limited | Natco Pharma Limited-Pharma Division | Natco Pharma Limited | Natco Pharma Limited-Pharma Division | 2019-10-25 | Human Prescription Drug Label |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 63850-0021-1 | Trihexyphenidyl Hydrochloride | 100 in 1 BOTTLE | TABLET | 100 | 2 | |
| 63850-0021-2 | Trihexyphenidyl Hydrochloride | 250 in 1 BOTTLE | TABLET | 250 | 2 | |
| 63850-0021-3 | Trihexyphenidyl Hydrochloride | 1000 in 1 BOTTLE | TABLET | 1000 | 2 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 63850-0021 | TRIHEXYPHENIDYL HYDROCHLORIDE TABLET [NATCO PHARMA LIMITED] | 2 | Current NDC, Legacy NDC, 3 package rows | 20191101_b7e4200c-feff-4537-aad1-cf9989fd8c14.zip |
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|---|---|---|---|---|
| TRIHEXYPHENIDYL HYDROCHLORIDE | ACTIVE INGREDIENT | AO61G82577 | TRIHEXYPHENIDYL HYDROCHLORIDE (TRIHEXYPHENIDYL HYDROCHLORIDE ) TABLET [NATCO PHARMA LIMITED-PHARMA DIVISION] | 1 | |
| TRIHEXYPHENIDYL | ACTIVE MOIETY | 6RC5V8B7PO | TRIHEXYPHENIDYL HYDROCHLORIDE (TRIHEXYPHENIDYL HYDROCHLORIDE ) TABLET [NATCO PHARMA LIMITED-PHARMA DIVISION] | 1 | |
| CELLULOSE, MICROCRYSTALLINE | INACTIVE INGREDIENT | OP1R32D61U | TRIHEXYPHENIDYL HYDROCHLORIDE (TRIHEXYPHENIDYL HYDROCHLORIDE ) TABLET [NATCO PHARMA LIMITED-PHARMA DIVISION] | 1 | |
| MAGNESIUM STEARATE | INACTIVE INGREDIENT | 70097M6I30 | TRIHEXYPHENIDYL HYDROCHLORIDE (TRIHEXYPHENIDYL HYDROCHLORIDE ) TABLET [NATCO PHARMA LIMITED-PHARMA DIVISION] | 1 | |
| SODIUM STARCH GLYCOLATE TYPE A POTATO | INACTIVE INGREDIENT | 5856J3G2A2 | TRIHEXYPHENIDYL HYDROCHLORIDE (TRIHEXYPHENIDYL HYDROCHLORIDE ) TABLET [NATCO PHARMA LIMITED-PHARMA DIVISION] | 1 |
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| TRIHEXYPHENIDYL HYDROCHLORIDE | TRIHEXYPHENIDYL HYDROCHLORIDE | REMEDYREPACK INC. | c25ea809-5bdf-4917-97f1-610059fbd0b7 | 2026-07-23 | Warnings, Adverse reactions | 905283 AO61G82577 |
| TRIHEXYPHENIDYL HYDROCHLORIDE | TRIHEXYPHENIDYL HYDROCHLORIDE | REMEDYREPACK INC. | b60ef86c-b8b6-4530-baaf-d4671ce961af | 2026-07-23 | Warnings, Adverse reactions | 905269 AO61G82577 |
| Trihexyphenidyl Hydrochloride | TRIHEXYPHENIDYL HYDROCHLORIDE | Chartwell RX, LLC | e8e2ac3b-80dc-4449-9365-2586d6d57e10 | 2026-07-17 | Warnings, Adverse reactions | AO61G82577 |
| Trihexyphenidyl Hydrochloride | TRIHEXYPHENIDYL HYDROCHLORIDE | REMEDYREPACK INC. | 86a65e8a-10f4-4f12-8e65-2edf398daeaa | 2026-07-09 | Warnings, Adverse reactions | 905269 AO61G82577 |
| Trihexyphenidyl Hydrochloride | TRIHEXYPHENIDYL HYDROCHLORIDE | REMEDYREPACK INC. | 3e71b957-9495-4583-8f00-99eac715ff85 | 2026-07-09 | Warnings, Adverse reactions | 905283 AO61G82577 |
| Trihexyphenidyl Hydrochloride | TRIHEXYPHENIDYL HYDROCHLORIDE | REMEDYREPACK INC. | 3ed3cdf1-1745-4c6f-bb90-fb7d9471270d | 2026-07-02 | Warnings, Adverse reactions | 905283 AO61G82577 |
| Trihexyphenidyl Hydrochloride | TRIHEXYPHENIDYL HYDROCHLORIDE | Bionpharma Inc. | 4d4d473e-4f84-43e7-bb17-49e8dc1e97fd | 2025-07-02 | Warnings, Adverse reactions | ANDA091630 905283 905269 AO61G82577 |
| YVTYVT MICRODERMABRASION FACIAL SCRUB | YVTYVT MICRODERMABRASION FACIAL SCRUB | Beijing JUNGE Technology Co., Ltd. | 2f30fc45-42e2-c766-e063-6394a90a8d68 | 2025-02-28 | Warnings | OP1R32D61U |
| Trihexyphenidyl Hydrochloride | TRIHEXYPHENIDYL HYDROCHLORIDE | PAI Holdings, LLC dba PAI Pharma | 9036c9f0-6d2d-4d0f-a20e-e36f9be228f7 | 2024-11-19 | Warnings, Adverse reactions | AO61G82577 |
| Trihexyphenidyl Hydrochloride | TRIHEXYPHENIDYL HYDROCHLORIDE | Actavis Pharma, Inc. | a44d7803-164d-4a67-9356-581c45de8596 | 2024-02-02 | Warnings, Adverse reactions | 905283 905269 AO61G82577 |
| TRIHEXYPHENIDYL HYDROCHLORIDE | TRIHEXYPHENIDYL HYDROCHLORIDE | Golden State Medical Supply Inc. | 9040cb3b-13d2-e46d-e053-2a95a90ae9e6 | 2023-09-26 | Warnings, Adverse reactions | 905283 905269 AO61G82577 |
| Trihexyphenidyl Hydrochloride | TRIHEXYPHENIDYL HYDROCHLORIDE | Akorn | 294cd88d-d9e8-4938-b4be-c3adc4a35de0 | 2022-06-21 | Warnings, Adverse reactions | AO61G82577 |
| Trihexyphenidyl Hydrochloride | TRIHEXYPHENIDYL HYDROCHLORIDE | Natco Pharma Limited | b7e4200c-feff-4537-aad1-cf9989fd8c14 | 2019-10-25 | Warnings, Adverse reactions | ANDA091630 63850-0022-2 63850-0022-1 63850-0021-2 63850-0021-3 63850-0021-1 63850-0022 63850-0021 63850002102 905283 905269 2b77cfd6-ad8a-4cbf-a22c-eb69e7a8548c b7e4200c-feff-4537-aad1-cf9989fd8c14 AO61G82577 |
| TRIHEXYPHENIDYL HYDROCHLORIDE | TRIHEXYPHENIDYL HYDROCHLORIDE | Novitium Pharma LLC | 83608c13-509d-448b-8559-5f5e8a9a0d75 | 2019-01-28 | Warnings, Adverse reactions | 905283 905269 AO61G82577 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.