Isoniazid
- Product NDC
- 43063-710
- 11-digit product format
- 430630710
- Labeler code
- 43063
- Product ID
- 43063-710_8010e7ac-6e5e-5f2c-e053-2991aa0a3767
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Isoniazid
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Application
- NDA008678
- Marketing category
- NDA
- Marketing start
- 1978-12-11
- Marketing end
- 2020-06-30
- Substance
- ISONIAZID
- Active strength
- 300 mg/1
- Pharmacologic classes
- Antimycobacterial [EPC]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record