Details for New Drug Application (NDA): 017584
✉ Email this page to a colleague
NDA 017584 describes LIDOCAINE HYDROCHLORIDE PRESERVATIVE FREE, which is a drug marketed by Eugia Pharma, Extrovis, Fresenius Kabi Usa, Hikma, Hospira, and Intl Medication, and is included in nine NDAs. It is available from ten suppliers. Additional details are available on the LIDOCAINE HYDROCHLORIDE PRESERVATIVE FREE profile page.
The generic ingredient in LIDOCAINE HYDROCHLORIDE PRESERVATIVE FREE is lidocaine hydrochloride. There are twenty-nine drug master file entries for this compound. Fifty-six suppliers are listed for this compound. Additional details are available on the lidocaine hydrochloride profile page.
The generic ingredient in LIDOCAINE HYDROCHLORIDE PRESERVATIVE FREE is lidocaine hydrochloride. There are twenty-nine drug master file entries for this compound. Fifty-six suppliers are listed for this compound. Additional details are available on the lidocaine hydrochloride profile page.
Summary for 017584
| Tradename: | LIDOCAINE HYDROCHLORIDE PRESERVATIVE FREE |
| Applicant: | Fresenius Kabi Usa |
| Ingredient: | lidocaine hydrochloride |
| Patents: | 0 |
Pharmacology for NDA: 017584
| Physiological Effect | Local Anesthesia |
Suppliers and Packaging for NDA: 017584
| Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
|---|---|---|---|---|---|---|---|---|
| LIDOCAINE HYDROCHLORIDE PRESERVATIVE FREE | lidocaine hydrochloride | INJECTABLE;INJECTION | 017584 | NDA | HF Acquisition Co LLC, DBA HealthFirst | 51662-1364 | 51662-1364-1 | 5 mL in 1 VIAL, SINGLE-DOSE (51662-1364-1) |
| LIDOCAINE HYDROCHLORIDE PRESERVATIVE FREE | lidocaine hydrochloride | INJECTABLE;INJECTION | 017584 | NDA | HF Acquisition Co LLC, DBA HealthFirst | 51662-1364 | 51662-1364-3 | 25 POUCH in 1 CASE (51662-1364-3) / 1 VIAL, SINGLE-DOSE in 1 POUCH (51662-1364-2) / 5 mL in 1 VIAL, SINGLE-DOSE |
Profile for product number 001
| Active Rx/OTC/Discontinued: | RX | Dosage: | INJECTABLE;INJECTION | Strength | 2% | ||||
| Approval Date: | Approved Prior to Jan 1, 1982 | TE: | AP | RLD: | No | ||||
Profile for product number 002
| Active Rx/OTC/Discontinued: | RX | Dosage: | INJECTABLE;INJECTION | Strength | 4% | ||||
| Approval Date: | Approved Prior to Jan 1, 1982 | TE: | AP | RLD: | No | ||||
Complete Access Available with Subscription
