Trihexyphenidyl Hydrochloride
- Product NDC
- 69452-242
- 11-digit product format
- 694520242
- Labeler code
- 69452
- Product ID
- 69452-242_4d4d473e-4f84-43e7-bb17-49e8dc1e97fd
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Trihexyphenidyl Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bionpharma Inc.
- Application
- ANDA091630
- Marketing category
- ANDA
- Marketing start
- 2018-12-15
- Marketing end
- 0000-00-00
- Substance
- TRIHEXYPHENIDYL HYDROCHLORIDE
- Active strength
- 5 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 69452-242-20 | Trihexyphenidyl Hydrochloride | 100 in 1 BOTTLE | TABLET | 100 | | 3 |
| 69452-242-32 | Trihexyphenidyl Hydrochloride | 1000 in 1 BOTTLE | TABLET | 1000 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 69452-242 | TRIHEXYPHENIDYL HYDROCHLORIDE TABLET [BIONPHARMA INC.] | 2 | Legacy NDC, 2 package rows | 20250114_4d4d473e-4f84-43e7-bb17-49e8dc1e97fd.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 |
|---|
| 69452-242-20 | 69452024220 | 100 TABLET in 1 BOTTLE (69452-242-20) | 100 tablet | 2018-12-15 | 0000-00-00 | No | No | Current |
| 69452-242-32 | 69452024232 | 1000 TABLET in 1 BOTTLE (69452-242-32) | 1000 tablet | 2018-12-15 | 0000-00-00 | No | No | Current |