Trihexyphenidyl Hydrochloride
- Product NDC
- 70518-1657
- 11-digit product format
- 705181657
- Labeler code
- 70518
- Product ID
- 70518-1657_494a509a-024c-be2e-e063-6294a90a9b34
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Trihexyphenidyl Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA084364
- Marketing category
- ANDA
- Marketing start
- 2018-11-09
- Substance
- TRIHEXYPHENIDYL HYDROCHLORIDE
- Active strength
- 5 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Trihexyphenidyl Hydrochloride
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| TRIHEXYPHENIDYL HYDROCHLORIDE | 5 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | AO61G82577 |
| Rxcui | 905283 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 70518-1657-0 | Trihexyphenidyl Hydrochloride | 30 in 1 BLISTER PACK | TABLET | 30 | | 12 |
| 70518-1657-1 | Trihexyphenidyl Hydrochloride | 100 in 1 BOX | TABLET | 100 | | 12 |
| 70518-1657-2 | Trihexyphenidyl Hydrochloride | 1 in 1 POUCH | TABLET | 1 | | 12 |
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 |
|---|
| 70518-1657-0 | 70518165700 | 30 TABLET in 1 BLISTER PACK (70518-1657-0) | 30 tablet | 2018-11-09 | 0000-00-00 | No | No | Current |
| 70518-1657-1 | 70518165701 | 100 POUCH in 1 BOX (70518-1657-1) / 1 TABLET in 1 POUCH (70518-1657-2) | 100 pouch | 2019-01-23 | 0000-00-00 | No | No | Current |
| 70518-1657-2 | 70518165702 | 1 in 1 POUCH | | | | | | Historical |