Myambutol
- Product NDC
- 70518-2691
- 11-digit product format
- 705182691
- Labeler code
- 70518
- Product ID
- 70518-2691_d6e59f75-cd3c-3fc4-e053-2a95a90abf4c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ethambutol hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- NDA016320
- Marketing category
- NDA
- Marketing start
- 2020-04-14
- Marketing end
- 0000-00-00
- Substance
- ETHAMBUTOL HYDROCHLORIDE
- Active strength
- 400 mg/1
- Pharmacologic classes
- Antimycobacterial [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- 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 |
|---|
| 70518-2691-0 | 70518269100 | 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-2691-0) | 2020-04-14 | 0000-00-00 | No | No | Current |