Ethambutol Hydrochloride
- Product NDC
- 0555-0923
- 11-digit product format
- 005550923
- Labeler code
- 0555
- Product ID
- 0555-0923_0794bcbd-6727-4d71-805e-b35de645b950
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ethambutol Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Teva Pharmaceuticals USA, Inc.
- Application
- ANDA076057
- Marketing category
- ANDA
- Marketing start
- 2001-11-27
- Marketing end
- 2021-10-31
- Substance
- ETHAMBUTOL HYDROCHLORIDE
- Active strength
- 400 mg/1
- Pharmacologic classes
- Antimycobacterial [EPC]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0555-0923-02 | 00555092302 | 100 TABLET, FILM COATED in 1 BOTTLE (0555-0923-02) | 2001-11-27 | 2021-10-31 | No | No | Current |