Details for New Drug Application (NDA): 216244
✉ Email this page to a colleague
NDA 216244 describes ESMOLOL HYDROCHLORIDE, which is a drug marketed by Am Regent, Amneal, Eugia Pharma, Fresenius Kabi Usa, Gland, Hikma, Hq Spclt Pharma, Mylan Institutional, Mylan Labs Ltd, and Sagent Pharms Inc, and is included in twelve NDAs. It is available from twelve suppliers. There are two patents protecting this drug. Additional details are available on the ESMOLOL HYDROCHLORIDE profile page.
The generic ingredient in ESMOLOL HYDROCHLORIDE is esmolol hydrochloride. There are eight drug master file entries for this compound. Fourteen suppliers are listed for this compound. Additional details are available on the esmolol hydrochloride profile page.
The generic ingredient in ESMOLOL HYDROCHLORIDE is esmolol hydrochloride. There are eight drug master file entries for this compound. Fourteen suppliers are listed for this compound. Additional details are available on the esmolol hydrochloride profile page.
Summary for 216244
| Tradename: | ESMOLOL HYDROCHLORIDE |
| Applicant: | Eugia Pharma |
| Ingredient: | esmolol hydrochloride |
| Patents: | 0 |
Pharmacology for NDA: 216244
| Mechanism of Action | Adrenergic beta-Antagonists |
Suppliers and Packaging for NDA: 216244
| Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
|---|---|---|---|---|---|---|---|---|
| ESMOLOL HYDROCHLORIDE | esmolol hydrochloride | INJECTABLE;INJECTION | 216244 | ANDA | Eugia US LLC | 55150-420 | 55150-420-10 | 10 POUCH in 1 CARTON (55150-420-10) / 1 BAG in 1 POUCH (55150-420-01) / 250 mL in 1 BAG |
| ESMOLOL HYDROCHLORIDE | esmolol hydrochloride | INJECTABLE;INJECTION | 216244 | ANDA | Eugia US LLC | 55150-421 | 55150-421-10 | 10 POUCH in 1 CARTON (55150-421-10) / 1 BAG in 1 POUCH (55150-421-01) / 100 mL in 1 BAG |
Profile for product number 001
| Active Rx/OTC/Discontinued: | RX | Dosage: | INJECTABLE;INJECTION | Strength | 1GM/100ML | ||||
| Approval Date: | Mar 21, 2022 | TE: | AP | RLD: | No | ||||
Profile for product number 002
| Active Rx/OTC/Discontinued: | RX | Dosage: | INJECTABLE;INJECTION | Strength | 2GM/100ML | ||||
| Approval Date: | Mar 21, 2022 | TE: | AP | RLD: | No | ||||
Complete Access Available with Subscription
