Trihexyphenidyl Hydrochloride
- Product NDC
- 70518-2880
- 11-digit product format
- 705182880
- Labeler code
- 70518
- Product ID
- 70518-2880_dd019ac9-1f94-767f-e053-2a95a90ab209
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Trihexyphenidyl Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA091630
- Marketing category
- ANDA
- Marketing start
- 2020-09-14
- Marketing end
- 0000-00-00
- Substance
- TRIHEXYPHENIDYL HYDROCHLORIDE
- Active strength
- 5 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-2880-0 | 70518288000 | 100 POUCH in 1 BOX (70518-2880-0) > 1 TABLET in 1 POUCH (70518-2880-1) | 100 pouch | 2020-09-14 | 0000-00-00 | No | No | Current |
| 70518-2880-2 | 70518288002 | 30 TABLET in 1 BLISTER PACK (70518-2880-2) | 30 tablet | 2021-04-06 | 0000-00-00 | No | No | Current |