Ethambutol Hydrochloride
- Product NDC
- 50090-5140
- 11-digit product format
- 500905140
- Labeler code
- 50090
- Product ID
- 50090-5140_8a4c2916-a557-4e37-a219-e108ff9e52d6
- 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
- 2009-07-10
- Marketing end
- 0000-00-00
- Substance
- ETHAMBUTOL HYDROCHLORIDE
- Active strength
- 100 mg/1
- Pharmacologic classes
- Antimycobacterial [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-5140-0 | 50090514000 | 100 TABLET in 1 BOTTLE (50090-5140-0) | 100 tablet | 2020-09-01 | 0000-00-00 | No | No | Current |
| 50090-5140-1 | 50090514001 | 60 TABLET in 1 BOTTLE (50090-5140-1) | 60 tablet | 2020-09-01 | 0000-00-00 | No | No | Current |