Trimethobenzamide Hydrochloride
- Product NDC
- 21695-448
- 11-digit product format
- 216950448
- Labeler code
- 21695
- Product ID
- 21695-448_c6a941a0-67dd-4c2a-accd-3a4578bc409c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Trimethobenzamide
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Rebel Distributors Corp.
- Application
- ANDA076570
- Marketing category
- ANDA
- Marketing start
- 2003-08-28
- Marketing end
- 0000-00-00
- Substance
- TRIMETHOBENZAMIDE HYDROCHLORIDE
- Active strength
- 300 mg/1
- Pharmacologic classes
- Antiemetic [EPC],Emesis Suppression [PE]
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 21695-448-10 | Trimethobenzamide Hydrochloride | 10 in 1 BOTTLE, PLASTIC | CAPSULE | 10 | | 1 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 21695-448 | TRIMETHOBENZAMIDE HYDROCHLORIDE (TRIMETHOBENZAMIDE) CAPSULE [REBEL DISTRIBUTORS CORP.] | 1 | Legacy NDC, 1 package rows | 20100105_43a47783-c605-49eb-a4fa-8524e75e69de.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 21695-448-10 | 21695044810 | 10 in 1 BOTTLE, PLASTIC | Historical |