Ethambutol Hydrochloride
- Product NDC
- 68151-0149
- 11-digit product format
- 681510149
- Labeler code
- 68151
- Product ID
- 68151-0149_fd2e7810-b660-41ab-a6c9-358243d18c37
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ethambutol Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Carilion Materials Management
- Application
- ANDA078939
- Marketing category
- ANDA
- Marketing start
- 2009-07-04
- Marketing end
- 0000-00-00
- Substance
- ETHAMBUTOL HYDROCHLORIDE
- Active strength
- 100 mg/1
- Pharmacologic classes
- Antimycobacterial [EPC]
- NDC exclude flag
- E
- Listing certified through
- 2018-12-31
- 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 |
|---|
| 68151-0149-0 | Ethambutol Hydrochloride | 1 in 1 PACKAGE | TABLET | 1 | | 4 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 68151-0149 | ETHAMBUTOL HYDROCHLORIDE TABLET [CARILION MATERIALS MANAGEMENT] | 4 | Legacy NDC, 1 package rows | 20170706_bb430cdb-ba6a-4b14-acb2-fbccdbf735d6.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 68151-0149-0 | 68151014900 | 1 in 1 PACKAGE | Historical |