Details for New Drug Application (NDA): 211370
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The generic ingredient in VERAPAMIL HYDROCHLORIDE is verapamil hydrochloride. There are seventeen drug master file entries for this compound. Forty-four suppliers are listed for this compound. Additional details are available on the verapamil hydrochloride profile page.
Summary for 211370
Tradename: | VERAPAMIL HYDROCHLORIDE |
Applicant: | Micro Labs |
Ingredient: | verapamil hydrochloride |
Patents: | 0 |
Formulation / Manufacturing: | see details |
Suppliers and Packaging for NDA: 211370
Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
---|---|---|---|---|---|---|---|---|
VERAPAMIL HYDROCHLORIDE | verapamil hydrochloride | SOLUTION;INTRAVENOUS | 211370 | ANDA | Micro Labs Limited | 42571-313 | 42571-313-75 | 1 VIAL in 1 CARTON (42571-313-75) / 2 mL in 1 VIAL |
VERAPAMIL HYDROCHLORIDE | verapamil hydrochloride | SOLUTION;INTRAVENOUS | 211370 | ANDA | Micro Labs Limited | 42571-313 | 42571-313-86 | 1 VIAL in 1 CARTON (42571-313-86) / 4 mL in 1 VIAL |
Profile for product number 001
Active Rx/OTC/Discontinued: | RX | Dosage: | SOLUTION;INTRAVENOUS | Strength | 5MG/2ML (2.5MG/ML) | ||||
Approval Date: | Dec 28, 2018 | TE: | AP | RLD: | No |
Profile for product number 002
Active Rx/OTC/Discontinued: | RX | Dosage: | SOLUTION;INTRAVENOUS | Strength | 10MG/4ML (2.5MG/ML) | ||||
Approval Date: | Dec 28, 2018 | TE: | AP | RLD: | No |
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