Isoniazid
- Product NDC
- 70518-0096
- 11-digit product format
- 705180096
- Labeler code
- 70518
- Product ID
- 70518-0096_ed985dfd-57ef-7da6-e053-2995a90a3ab1
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Isoniazid
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA080936
- Marketing category
- ANDA
- Marketing start
- 2016-12-30
- Marketing end
- 0000-00-00
- Substance
- ISONIAZID
- Active strength
- 100 mg/1
- Pharmacologic classes
- Antimycobacterial [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-0096-0 | 70518009600 | 30 TABLET in 1 BOTTLE (70518-0096-0) | 30 tablet | 2016-12-30 | 0000-00-00 | No | No | Current |