Details for New Drug Application (NDA): 212857
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The generic ingredient in DEXMEDETOMIDINE HYDROCHLORIDE is dexmedetomidine hydrochloride. There are fourteen drug master file entries for this compound. Thirty suppliers are listed for this compound. Additional details are available on the dexmedetomidine hydrochloride profile page.
Summary for 212857
Tradename: | DEXMEDETOMIDINE HYDROCHLORIDE |
Applicant: | Tagi |
Ingredient: | dexmedetomidine hydrochloride |
Patents: | 0 |
Pharmacology for NDA: 212857
Mechanism of Action | Adrenergic alpha2-Agonists |
Physiological Effect | General Anesthesia |
Medical Subject Heading (MeSH) Categories for 212857
Suppliers and Packaging for NDA: 212857
Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
---|---|---|---|---|---|---|---|---|
DEXMEDETOMIDINE HYDROCHLORIDE | dexmedetomidine hydrochloride | INJECTABLE;INJECTION | 212857 | ANDA | Precision Dose, Inc. | 68094-047 | 68094-047-10 | 10 VIAL in 1 CARTON (68094-047-10) / 20 mL in 1 VIAL (68094-047-01) |
DEXMEDETOMIDINE HYDROCHLORIDE | dexmedetomidine hydrochloride | INJECTABLE;INJECTION | 212857 | ANDA | Precision Dose, Inc. | 68094-147 | 68094-147-20 | 20 BOTTLE in 1 CARTON (68094-147-20) / 50 mL in 1 BOTTLE (68094-147-01) |
Profile for product number 001
Active Rx/OTC/Discontinued: | RX | Dosage: | INJECTABLE;INJECTION | Strength | EQ 80MCG BASE/20ML (EQ 4MCG BASE/ML) | ||||
Approval Date: | Nov 23, 2020 | TE: | AP | RLD: | No |
Profile for product number 002
Active Rx/OTC/Discontinued: | RX | Dosage: | INJECTABLE;INJECTION | Strength | EQ 200MCG BASE/50ML (EQ 4MCG BASE/ML) | ||||
Approval Date: | Nov 23, 2020 | TE: | AP | RLD: | No |
Profile for product number 003
Active Rx/OTC/Discontinued: | RX | Dosage: | INJECTABLE;INJECTION | Strength | EQ 400MCG BASE/100ML (EQ 4MCG BASE/ML) | ||||
Approval Date: | Nov 23, 2020 | TE: | AP | RLD: | No |
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