NDC 70518-2878-1 - 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
- 70518-2878
- Requested NDC
- 70518-2878-1
- Package NDCs from labels
- 70518-2878-1, 70518-2878-0
- Manufacturer
- REMEDYREPACK INC.
- Effective date
- 2023-09-08
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Trihexyphenidyl Hydrochloride - REMEDYREPACK INC. | REMEDYREPACK INC. | 2023-09-08 | HUMAN PRESCRIPTION DRUG LABEL |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 70518-2878-0 | 2022-02-08 | C162847 | 48780-1 | d6a99b39-7bab-a426-e053-dadaa90af4c2 | 64e73695-8aba-4715-845a-05b4e8de72b0 |
| 70518-2878-0 | 2022-01-28 | C162847 | 48780-1 | d6a99b39-7bab-a426-e053-dadaa90af4c2 | 64e73695-8aba-4715-845a-05b4e8de72b0 |
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 | AO61G82577 |
| TRIHEXYPHENIDYL HYDROCHLORIDE | TRIHEXYPHENIDYL HYDROCHLORIDE | REMEDYREPACK INC. | b60ef86c-b8b6-4530-baaf-d4671ce961af | 2026-07-23 | Warnings, Adverse reactions | 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 | AO61G82577 |
| Trihexyphenidyl Hydrochloride | TRIHEXYPHENIDYL HYDROCHLORIDE | REMEDYREPACK INC. | 3e71b957-9495-4583-8f00-99eac715ff85 | 2026-07-09 | Warnings, Adverse reactions | AO61G82577 |
| Trihexyphenidyl Hydrochloride | TRIHEXYPHENIDYL HYDROCHLORIDE | REMEDYREPACK INC. | 3ed3cdf1-1745-4c6f-bb90-fb7d9471270d | 2026-07-02 | Warnings, Adverse reactions | AO61G82577 |
| Trihexyphenidyl Hydrochloride | TRIHEXYPHENIDYL HYDROCHLORIDE | Bionpharma Inc. | 4d4d473e-4f84-43e7-bb17-49e8dc1e97fd | 2025-07-02 | Warnings, Adverse reactions | ANDA091630 69452-241 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 | AO61G82577 |
| 09418ead-b90e-ce61-e063-6394a90ad3ce | 64e73695-8aba-4715-845a-05b4e8de72b0 | 2023-11-03 | Warnings, Adverse reactions | 64e73695-8aba-4715-845a-05b4e8de72b0 | ||
| TRIHEXYPHENIDYL HYDROCHLORIDE | TRIHEXYPHENIDYL HYDROCHLORIDE | Golden State Medical Supply Inc. | 9040cb3b-13d2-e46d-e053-2a95a90ae9e6 | 2023-09-26 | Warnings, Adverse reactions | 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 AO61G82577 |
| TRIHEXYPHENIDYL HYDROCHLORIDE | TRIHEXYPHENIDYL HYDROCHLORIDE | Novitium Pharma LLC | 83608c13-509d-448b-8559-5f5e8a9a0d75 | 2019-01-28 | Warnings, Adverse reactions | AO61G82577 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.