Isoniazid
- Product NDC
- 68788-8927
- 11-digit product format
- 687888927
- Labeler code
- 68788
- Product ID
- 68788-8927_d13831c5-bb00-4721-9f80-8152ce1cdc74
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Isoniazid
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals Inc.
- Application
- NDA008678
- Marketing category
- NDA
- Marketing start
- 2015-10-07
- Marketing end
- 0000-00-00
- Substance
- ISONIAZID
- Active strength
- 300 mg/1
- Pharmacologic classes
- Antimycobacterial [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record