Bupivacaine Hydrochloride

Product NDC

70518-2040

11-digit product format

705182040

Labeler code

70518

Product ID

70518-2040_970f15aa-fafe-7a7f-e053-2995a90ae5ea

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

BUPIVACAINE HYDROCHLORIDE

Dosage form

INJECTION, SOLUTION

Route

EPIDURAL; INTRACAUDAL; PERINEURAL

Labeler

REMEDYREPACK INC.

Application

ANDA070584

Marketing category

ANDA

Marketing start

2019-04-26

Marketing end

0000-00-00

Substance

BUPIVACAINE HYDROCHLORIDE

Active strength

5 mg/mL

Pharmacologic classes

Amide Local Anesthetic [EPC],Amides [CS],Local Anesthesia [PE]

NDC exclude flag

No

Listing certified through

2020-12-31

Current FDA listing

Historical FDA.report record