Details for New Drug Application (NDA): 211849
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The generic ingredient in CHLORZOXAZONE is chlorzoxazone. There are sixteen drug master file entries for this compound. Twenty suppliers are listed for this compound. Additional details are available on the chlorzoxazone profile page.
Summary for 211849
| Tradename: | CHLORZOXAZONE |
| Applicant: | Dr Reddys Labs Sa |
| Ingredient: | chlorzoxazone |
| Patents: | 0 |
Pharmacology for NDA: 211849
| Physiological Effect | Centrally-mediated Muscle Relaxation |
Medical Subject Heading (MeSH) Categories for 211849
Suppliers and Packaging for NDA: 211849
| Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
|---|---|---|---|---|---|---|---|---|
| CHLORZOXAZONE | chlorzoxazone | TABLET;ORAL | 211849 | ANDA | Mayne Pharma Commercial LLC | 51862-339 | 51862-339-01 | 100 TABLET in 1 BOTTLE (51862-339-01) |
Profile for product number 001
| Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | 375MG | ||||
| Approval Date: | Jul 21, 2020 | TE: | AB | RLD: | No | ||||
Profile for product number 002
| Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | 500MG | ||||
| Approval Date: | Jul 21, 2020 | TE: | AA | RLD: | No | ||||
Profile for product number 003
| Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | 750MG | ||||
| Approval Date: | Jul 21, 2020 | TE: | AB | RLD: | No | ||||
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