Tetrabenazine
- Product NDC
- 42291-806
- 11-digit product format
- 422910806
- Labeler code
- 42291
- Product ID
- 42291-806_d5c9e83d-60d5-fb9c-e053-2995a90a9731
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Tetrabenazine
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- AvKARE
- Application
- ANDA207682
- Marketing category
- ANDA
- Marketing start
- 2017-02-08
- Marketing end
- 0000-00-00
- Substance
- TETRABENAZINE
- Active strength
- 13 mg/1
- Pharmacologic classes
- Vesicular Monoamine Transporter 2 Inhibitor [EPC], Vesicular Monoamine Transporter 2 Inhibitors [MoA]
- 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 |
|---|
| 42291-806-30 | 42291080630 | 30 TABLET in 1 BOTTLE (42291-806-30) | 30 tablet | 2017-02-08 | 0000-00-00 | No | No | Current |