Myambutol
- Product NDC
- 50090-2607
- 11-digit product format
- 500902607
- Labeler code
- 50090
- Product ID
- 50090-2607_4231c828-3f03-4b08-807c-b0b3b35af082
- 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
- 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 | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-2607-0 | 50090260700 | 100 TABLET, FILM COATED in 1 BOTTLE (50090-2607-0) | 2016-11-09 | 0000-00-00 | No | No | Current |