Ethambutol Hydrochloride
- Product NDC
- 70518-0459
- 11-digit product format
- 705180459
- Labeler code
- 70518
- Product ID
- 70518-0459_a47eb2c0-c2a4-5841-e053-2a95a90a1fd7
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ethambutol Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- NDA016320
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 2017-04-25
- Marketing end
- 0000-00-00
- Substance
- ETHAMBUTOL HYDROCHLORIDE
- Active strength
- 400 mg/1
- Pharmacologic classes
- Antimycobacterial [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- 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 |
|---|
| 70518-0459-0 | 70518045900 | 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-0459-0) | 2017-04-25 | 0000-00-00 | No | No | Current |