TETRABENAZINE
- Product NDC
- 69452-118
- 11-digit product format
- 694520118
- Labeler code
- 69452
- Product ID
- 69452-118_0fb2ef1a-8abf-38b2-e063-6394a90a6cee
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- TETRABENAZINE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bionpharma Inc.
- Application
- ANDA208826
- Marketing category
- ANDA
- Marketing start
- 2018-01-15
- Substance
- TETRABENAZINE
- Active strength
- 25 mg/1
- Pharmacologic classes
- Vesicular Monoamine Transporter 2 Inhibitor [EPC], Vesicular Monoamine Transporter 2 Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- TETRABENAZINE
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| TETRABENAZINE | 25 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | Z9O08YRN8O |
| Rxcui | 199592, 805464 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 69452-118-21 | TETRABENAZINE | 112 in 1 BOTTLE | TABLET | 112 | | 5 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 69452-118 | TETRABENAZINE TABLET [BIONPHARMA INC.] | 5 | Current NDC, Legacy NDC, 1 package rows | 20240126_acf78d97-fca5-49aa-8683-6db7396da72f.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 69452-118-21 | 69452011821 | 112 TABLET in 1 BOTTLE (69452-118-21) | 112 tablet | 2018-01-15 | 0000-00-00 | No | No | Current |