Isoniazid
- Product NDC
- 70518-2576
- 11-digit product format
- 705182576
- Labeler code
- 70518
- Product ID
- 70518-2576_eafe8571-7adb-2faf-e053-2a95a90a959e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Isoniazid
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA080937
- Marketing category
- ANDA
- Marketing start
- 2020-02-13
- Marketing end
- 0000-00-00
- Substance
- ISONIAZID
- Active strength
- 300 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 | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 70518-2576-0 | 70518257600 | 30 TABLET in 1 BLISTER PACK (70518-2576-0) | 30 tablet | 2020-02-13 | 0000-00-00 | No | No | Current |
| 70518-2576-1 | 70518257601 | 30 TABLET in 1 BOTTLE, PLASTIC (70518-2576-1) | 30 tablet | 2020-06-17 | 0000-00-00 | No | No | Current |