Trihexyphenidyl Hydrochloride
- Product NDC
- 70518-2878
- 11-digit product format
- 705182878
- Labeler code
- 70518
- Product ID
- 70518-2878_d7834c55-72df-94eb-e053-2995a90a6d0f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Trihexyphenidyl Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA091630
- Marketing category
- ANDA
- Marketing start
- 2020-09-11
- Marketing end
- 0000-00-00
- Substance
- TRIHEXYPHENIDYL HYDROCHLORIDE
- Active strength
- 2 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-2878-0 | 70518287800 | 100 POUCH in 1 BOX (70518-2878-0) > 1 TABLET in 1 POUCH (70518-2878-1) | 100 pouch | 2020-09-11 | 0000-00-00 | No | No | Current |