Trihexyphenidyl Hydrochloride
- Product NDC
- 68151-2782
- 11-digit product format
- 681512782
- Labeler code
- 68151
- Product ID
- 68151-2782_76496d76-9d7a-4f3c-8915-94cd77bb2cb7
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Trihexyphenidyl Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Carilion Materials Management
- Application
- ANDA084363
- Marketing category
- ANDA
- Marketing start
- 1987-11-01
- Marketing end
- 0000-00-00
- Substance
- TRIHEXYPHENIDYL HYDROCHLORIDE
- Active strength
- 2 mg/1
- NDC exclude flag
- E
- Listing certified through
- 2018-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 68151-2782-7 | Trihexyphenidyl Hydrochloride | 1 in 1 BOTTLE | TABLET | 1 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 68151-2782 | TRIHEXYPHENIDYL HYDROCHLORIDE TABLET [CARILION MATERIALS MANAGEMENT] | 2 | Legacy NDC, 1 package rows | 20160229_b8ad285a-383a-46bc-90e8-8d58e9a01b94.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 68151-2782-7 | 68151278207 | 1 in 1 BOTTLE | Historical |