Details for New Drug Application (NDA): 040302
✉ Email this page to a colleague
NDA 040302 describes LIDOCAINE HYDROCHLORIDE PRESERVATIVE FREE IN PLASTIC CONTAINER, which is a drug marketed by Hospira and is included in one NDA. It is available from six suppliers. Additional details are available on the LIDOCAINE HYDROCHLORIDE PRESERVATIVE FREE IN PLASTIC CONTAINER profile page.
The generic ingredient in LIDOCAINE HYDROCHLORIDE PRESERVATIVE FREE IN PLASTIC CONTAINER is lidocaine hydrochloride. There are twenty-nine drug master file entries for this compound. Sixty-one suppliers are listed for this compound. Additional details are available on the lidocaine hydrochloride profile page.
The generic ingredient in LIDOCAINE HYDROCHLORIDE PRESERVATIVE FREE IN PLASTIC CONTAINER is lidocaine hydrochloride. There are twenty-nine drug master file entries for this compound. Sixty-one suppliers are listed for this compound. Additional details are available on the lidocaine hydrochloride profile page.
Summary for 040302
| Tradename: | LIDOCAINE HYDROCHLORIDE PRESERVATIVE FREE IN PLASTIC CONTAINER |
| Applicant: | Hospira |
| Ingredient: | lidocaine hydrochloride |
| Patents: | 0 |
Pharmacology for NDA: 040302
| Physiological Effect | Local Anesthesia |
Suppliers and Packaging for NDA: 040302
| Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
|---|---|---|---|---|---|---|---|---|
| LIDOCAINE HYDROCHLORIDE PRESERVATIVE FREE IN PLASTIC CONTAINER | lidocaine hydrochloride | INJECTABLE;INJECTION | 040302 | ANDA | Henry Schein, Inc. | 0404-9889 | 0404-9889-05 | 1 CARTON in 1 BAG (0404-9889-05) / 1 SYRINGE in 1 CARTON / 5 mL in 1 SYRINGE |
| LIDOCAINE HYDROCHLORIDE PRESERVATIVE FREE IN PLASTIC CONTAINER | lidocaine hydrochloride | INJECTABLE;INJECTION | 040302 | ANDA | Henry Schein, Inc. | 0404-9894 | 0404-9894-05 | 1 CARTON in 1 BAG (0404-9894-05) / 1 SYRINGE in 1 CARTON / 5 mL in 1 SYRINGE |
Profile for product number 001
| Active Rx/OTC/Discontinued: | RX | Dosage: | INJECTABLE;INJECTION | Strength | 1% | ||||
| Approval Date: | Sep 28, 1998 | TE: | AP | RLD: | No | ||||
Profile for product number 002
| Active Rx/OTC/Discontinued: | RX | Dosage: | INJECTABLE;INJECTION | Strength | 2% | ||||
| Approval Date: | Sep 28, 1998 | TE: | AP | RLD: | No | ||||
Complete Access Available with Subscription
