Trihexyphenidyl Hydrochloride
- Product NDC
- 50090-2994
- 11-digit product format
- 500902994
- Labeler code
- 50090
- Product ID
- 50090-2994_6184c8a1-d617-4937-a71e-48d238138d28
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Trihexyphenidyl Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- 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
- No
- Listing certified through
- 2022-12-31
- 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 |
|---|
| 50090-2994-0 | Trihexyphenidyl Hydrochloride | 32 in 1 BOX, UNIT-DOSE | TABLET | 32 | | 11 |
| 50090-2994-0 | Trihexyphenidyl Hydrochloride | 1 in 1 BLISTER PACK | TABLET | 1 | | 11 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-2994 | TRIHEXYPHENIDYL HYDROCHLORIDE TABLET [A-S MEDICATION SOLUTIONS] | 11 | Legacy NDC, 2 package rows | 20211109_e34e1be1-0d59-4625-85a3-babbb7cbd6b8.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-2994-0 | 50090299400 | 32 BLISTER PACK in 1 BOX, UNIT-DOSE (50090-2994-0) > 1 TABLET in 1 BLISTER PACK | 32 blister pack | 2017-04-28 | 0000-00-00 | No | No | Current |