Ethambutol Hydrochloride
- Product NDC
- 50090-5142
- 11-digit product format
- 500905142
- Labeler code
- 50090
- Product ID
- 50090-5142_5e1899b2-97e0-4d75-a318-25c47062693a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ethambutol Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA078939
- Marketing category
- ANDA
- Marketing start
- 2009-07-04
- Marketing end
- 0000-00-00
- Substance
- ETHAMBUTOL HYDROCHLORIDE
- Active strength
- 400 mg/1
- Pharmacologic classes
- Antimycobacterial [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- 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 |
|---|
| 50090-5142-0 | Ethambutol Hydrochloride | 100 in 1 BOTTLE | TABLET | 100 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-5142 | ETHAMBUTOL HYDROCHLORIDE TABLET [A-S MEDICATION SOLUTIONS] | 3 | Legacy NDC, 1 package rows | 20210615_8ee30365-adc1-4b93-b263-9f8b79223b02.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 |
|---|
| 50090-5142-0 | 50090514200 | 100 TABLET in 1 BOTTLE (50090-5142-0) | 100 tablet | 2020-09-02 | 0000-00-00 | No | No | Current |