Ethambutol Hydrochloride
- Product NDC
- 50090-2399
- 11-digit product format
- 500902399
- Labeler code
- 50090
- Product ID
- 50090-2399_64bfd6c1-932e-4d1f-8dd5-3358c853a31b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ethambutol Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- NDA016320
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 2006-12-15
- Marketing end
- 0000-00-00
- Substance
- ETHAMBUTOL HYDROCHLORIDE
- Active strength
- 400 mg/1
- Pharmacologic classes
- Antimycobacterial [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record