chlorzoxazone
- Product NDC
- 69597-330
- 11-digit product format
- 695970330
- Labeler code
- 69597
- Product ID
- 69597-330_9a96145a-6312-480c-8774-52f5901eab39
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- chlorzoxazone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Basiem
- Application
- ANDA207483
- Marketing category
- ANDA
- Marketing start
- 2019-07-30
- Marketing end
- 0000-00-00
- Substance
- CHLORZOXAZONE
- Active strength
- 250 mg/1
- Pharmacologic classes
- Centrally-mediated Muscle Relaxation [PE],Muscle Relaxant [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record