Myambutol
- Product NDC
- 50090-0417
- 11-digit product format
- 500900417
- Labeler code
- 50090
- Product ID
- 50090-0417_08960965-7698-4a28-ae3d-271a6baadc4f
- 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
- Marketing start
- 2007-08-10
- 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