Details for New Drug Application (NDA): 075138
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The generic ingredient in VERAPAMIL HYDROCHLORIDE is verapamil hydrochloride. There are seventeen drug master file entries for this compound. Forty-five suppliers are listed for this compound. Additional details are available on the verapamil hydrochloride profile page.
Summary for 075138
Tradename: | VERAPAMIL HYDROCHLORIDE |
Applicant: | Mylan |
Ingredient: | verapamil hydrochloride |
Patents: | 0 |
Suppliers and Packaging for NDA: 075138
Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
---|---|---|---|---|---|---|---|---|
VERAPAMIL HYDROCHLORIDE | verapamil hydrochloride | CAPSULE, EXTENDED RELEASE;ORAL | 075138 | ANDA | Mylan Pharmaceuticals Inc. | 0378-6320 | 0378-6320-01 | 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (0378-6320-01) |
VERAPAMIL HYDROCHLORIDE | verapamil hydrochloride | CAPSULE, EXTENDED RELEASE;ORAL | 075138 | ANDA | Mylan Pharmaceuticals Inc. | 0378-6380 | 0378-6380-01 | 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (0378-6380-01) |
Profile for product number 001
Active Rx/OTC/Discontinued: | RX | Dosage: | CAPSULE, EXTENDED RELEASE;ORAL | Strength | 120MG | ||||
Approval Date: | Apr 20, 1999 | TE: | AB | RLD: | No |
Profile for product number 002
Active Rx/OTC/Discontinued: | RX | Dosage: | CAPSULE, EXTENDED RELEASE;ORAL | Strength | 180MG | ||||
Approval Date: | Apr 20, 1999 | TE: | AB | RLD: | No |
Profile for product number 003
Active Rx/OTC/Discontinued: | RX | Dosage: | CAPSULE, EXTENDED RELEASE;ORAL | Strength | 240MG | ||||
Approval Date: | Apr 20, 1999 | TE: | AB | RLD: | No |
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