Trihexyphenidyl Hydrochloride
- Product NDC
- 16571-160
- 11-digit product format
- 165710160
- Labeler code
- 16571
- Product ID
- 16571-160_d443c56d-9361-4642-a2b5-9a12dab45af8
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Trihexyphenidyl Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Rising Pharmaceuticals, Inc.
- Application
- ANDA091630
- Marketing category
- ANDA
- Marketing start
- 2010-11-17
- Marketing end
- 0000-00-00
- Substance
- TRIHEXYPHENIDYL HYDROCHLORIDE
- Active strength
- 2 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- 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 |
|---|
| 16571-160-10 | 16571016010 | 100 TABLET in 1 BOTTLE (16571-160-10) | 100 tablet | 2010-11-17 | 0000-00-00 | No | No | Current |
| 16571-160-11 | 16571016011 | 1000 TABLET in 1 BOTTLE (16571-160-11) | 1000 tablet | 2010-11-17 | 0000-00-00 | No | No | Current |