Details for New Drug Application (NDA): 207314
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The generic ingredient in CYCLOBENZAPRINE HYDROCHLORIDE is cyclobenzaprine hydrochloride. There are sixteen drug master file entries for this compound. Sixty suppliers are listed for this compound. Additional details are available on the cyclobenzaprine hydrochloride profile page.
Summary for 207314
| Tradename: | CYCLOBENZAPRINE HYDROCHLORIDE |
| Applicant: | Macleods Pharms Ltd |
| Ingredient: | cyclobenzaprine hydrochloride |
| Patents: | 0 |
Pharmacology for NDA: 207314
| Physiological Effect | Centrally-mediated Muscle Relaxation |
Suppliers and Packaging for NDA: 207314
| Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
|---|---|---|---|---|---|---|---|---|
| CYCLOBENZAPRINE HYDROCHLORIDE | cyclobenzaprine hydrochloride | CAPSULE, EXTENDED RELEASE;ORAL | 207314 | ANDA | Macleods Pharmaceuticals Limited | 33342-272 | 33342-272-09 | 60 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (33342-272-09) |
| CYCLOBENZAPRINE HYDROCHLORIDE | cyclobenzaprine hydrochloride | CAPSULE, EXTENDED RELEASE;ORAL | 207314 | ANDA | Macleods Pharmaceuticals Limited | 33342-272 | 33342-272-12 | 10 BLISTER PACK in 1 CARTON (33342-272-12) / 10 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK |
Profile for product number 001
| Active Rx/OTC/Discontinued: | RX | Dosage: | CAPSULE, EXTENDED RELEASE;ORAL | Strength | 15MG | ||||
| Approval Date: | Jul 22, 2024 | TE: | AB | RLD: | No | ||||
Profile for product number 002
| Active Rx/OTC/Discontinued: | RX | Dosage: | CAPSULE, EXTENDED RELEASE;ORAL | Strength | 30MG | ||||
| Approval Date: | Jul 22, 2024 | TE: | AB | RLD: | No | ||||
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