Trihexyphenidyl Hydrochloride
- Product NDC
- 70518-3268
- 11-digit product format
- 705183268
- Labeler code
- 70518
- Product ID
- 70518-3268_d0ea3183-9f2f-13d4-e053-2995a90a6b63
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Trihexyphenidyl Hydrochloride
- Dosage form
- SOLUTION
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA040177
- Marketing category
- ANDA
- Marketing start
- 2021-11-15
- Marketing end
- 0000-00-00
- Substance
- TRIHEXYPHENIDYL HYDROCHLORIDE
- Active strength
- 2 mg/5mL
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70518-3268 | TRIHEXYPHENIDYL HYDROCHLORIDE SOLUTION [REMEDYREPACK INC.] | 8 | Legacy NDC | 20250522_1e98bd29-c339-4ede-841a-1b2834aaf48b.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-3268-0 | 70518326800 | 10 CUP, UNIT-DOSE in 1 BOX (70518-3268-0) > 12.5 mL in 1 CUP, UNIT-DOSE (70518-3268-1) | 2021-11-15 | 0000-00-00 | No | No | Current |