Details for New Drug Application (NDA): 208622
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The generic ingredient in TIZANIDINE HYDROCHLORIDE is tizanidine hydrochloride. There are eleven drug master file entries for this compound. Fifty-two suppliers are listed for this compound. Additional details are available on the tizanidine hydrochloride profile page.
Summary for 208622
Tradename: | TIZANIDINE HYDROCHLORIDE |
Applicant: | Zydus Pharms |
Ingredient: | tizanidine hydrochloride |
Patents: | 0 |
Pharmacology for NDA: 208622
Mechanism of Action | Adrenergic alpha2-Agonists |
Suppliers and Packaging for NDA: 208622
Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
---|---|---|---|---|---|---|---|---|
TIZANIDINE HYDROCHLORIDE | tizanidine hydrochloride | CAPSULE;ORAL | 208622 | ANDA | Quality Care Products, LLC | 55700-999 | 55700-999-30 | 30 CAPSULE in 1 BOTTLE (55700-999-30) |
TIZANIDINE HYDROCHLORIDE | tizanidine hydrochloride | CAPSULE;ORAL | 208622 | ANDA | Zydus Pharmaceuticals (USA) Inc. | 70710-1111 | 70710-1111-4 | 10 BLISTER PACK in 1 CARTON (70710-1111-4) / 10 CAPSULE in 1 BLISTER PACK |
Profile for product number 001
Active Rx/OTC/Discontinued: | RX | Dosage: | CAPSULE;ORAL | Strength | EQ 2MG BASE | ||||
Approval Date: | Mar 3, 2017 | TE: | AB | RLD: | No |
Profile for product number 002
Active Rx/OTC/Discontinued: | RX | Dosage: | CAPSULE;ORAL | Strength | EQ 4MG BASE | ||||
Approval Date: | Mar 3, 2017 | TE: | AB | RLD: | No |
Profile for product number 003
Active Rx/OTC/Discontinued: | RX | Dosage: | CAPSULE;ORAL | Strength | EQ 6MG BASE | ||||
Approval Date: | Mar 3, 2017 | TE: | AB | RLD: | No |
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