Details for New Drug Application (NDA): 040089
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The generic ingredient in ACETAZOLAMIDE SODIUM is acetazolamide sodium. There are ten drug master file entries for this compound. Six suppliers are listed for this compound. Additional details are available on the acetazolamide sodium profile page.
Summary for 040089
Tradename: | ACETAZOLAMIDE SODIUM |
Applicant: | Hikma |
Ingredient: | acetazolamide sodium |
Patents: | 0 |
Pharmacology for NDA: 040089
Mechanism of Action | Carbonic Anhydrase Inhibitors |
Suppliers and Packaging for NDA: 040089
Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
---|---|---|---|---|---|---|---|---|
ACETAZOLAMIDE SODIUM | acetazolamide sodium | INJECTABLE;INJECTION | 040089 | ANDA | Hikma Pharmaceuticals USA Inc. | 0143-9006 | 0143-9006-01 | 1 VIAL in 1 CARTON (0143-9006-01) / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL |
ACETAZOLAMIDE SODIUM | acetazolamide sodium | INJECTABLE;INJECTION | 040089 | ANDA | Hikma Pharmaceuticals USA Inc. | 0143-9503 | 0143-9503-01 | 1 VIAL in 1 BOX, UNIT-DOSE (0143-9503-01) / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL |
Profile for product number 001
Active Rx/OTC/Discontinued: | RX | Dosage: | INJECTABLE;INJECTION | Strength | EQ 500MG BASE/VIAL | ||||
Approval Date: | Feb 28, 1995 | TE: | AP | RLD: | No |
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