Details for New Drug Application (NDA): 207551
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The generic ingredient in DEXMEDETOMIDINE HYDROCHLORIDE is dexmedetomidine hydrochloride. There are fourteen drug master file entries for this compound. Twenty-nine suppliers are listed for this compound. Additional details are available on the dexmedetomidine hydrochloride profile page.
Summary for 207551
Tradename: | DEXMEDETOMIDINE HYDROCHLORIDE |
Applicant: | Amneal Pharms Co |
Ingredient: | dexmedetomidine hydrochloride |
Patents: | 0 |
Pharmacology for NDA: 207551
Mechanism of Action | Adrenergic alpha2-Agonists |
Physiological Effect | General Anesthesia |
Medical Subject Heading (MeSH) Categories for 207551
Suppliers and Packaging for NDA: 207551
Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
---|---|---|---|---|---|---|---|---|
DEXMEDETOMIDINE HYDROCHLORIDE | dexmedetomidine hydrochloride | INJECTABLE;INJECTION | 207551 | ANDA | Amneal Pharmaceuticals LLC | 70121-1388 | 70121-1388-8 | 20 BOTTLE, GLASS in 1 CARTON (70121-1388-8) / 50 mL in 1 BOTTLE, GLASS (70121-1388-1) |
DEXMEDETOMIDINE HYDROCHLORIDE | dexmedetomidine hydrochloride | INJECTABLE;INJECTION | 207551 | ANDA | Amneal Pharmaceuticals LLC | 70121-1389 | 70121-1389-7 | 10 BOTTLE, GLASS in 1 CARTON (70121-1389-7) / 100 mL in 1 BOTTLE, GLASS (70121-1389-1) |
Profile for product number 001
Active Rx/OTC/Discontinued: | RX | Dosage: | INJECTABLE;INJECTION | Strength | EQ 200MCG BASE/50ML (EQ 4MCG BASE/ML) | ||||
Approval Date: | May 20, 2020 | TE: | AP | RLD: | No |
Profile for product number 002
Active Rx/OTC/Discontinued: | RX | Dosage: | INJECTABLE;INJECTION | Strength | EQ 400MCG BASE/100ML (EQ 4MCG BASE/ML) | ||||
Approval Date: | May 20, 2020 | TE: | AP | RLD: | No |
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