CHLORZOXAZONE
- Product NDC
- 72319-168
- 11-digit product format
- 723190168
- Labeler code
- 72319
- Product ID
- 72319-168_7fc76bc9-380c-4b26-8a3e-b5f6ac956618
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- CHLORZOXAZONE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- i3 Pharmaceuticals, LLC
- Application
- ANDA212053
- Marketing category
- ANDA
- Marketing start
- 2020-09-16
- Marketing end
- 0000-00-00
- Substance
- CHLORZOXAZONE
- Active strength
- 750 mg/1
- Pharmacologic classes
- Centrally-mediated Muscle Relaxation [PE],Muscle Relaxant [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- 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 |
|---|
| 72319-168-04 | 72319016804 | 100 TABLET in 1 BOTTLE, PLASTIC (72319-168-04) | 100 tablet | 2020-09-16 | 0000-00-00 | No | No | Current |
| 72319-168-05 | 72319016805 | 500 TABLET in 1 BOTTLE, PLASTIC (72319-168-05) | 500 tablet | 2020-09-16 | 0000-00-00 | No | No | Current |