NDC 73293-0002 – Bupivacaine Hydrochloride

Bupivacaine Hydrochloride 7.5 mg/mL · Injection · Subarachnoid

Human Prescription Drug 1 recall

Product NDC73293-0002

Product details

Brand name
Bupivacaine Hydrochloride
Generic name
Bupivacaine hydrochloride
Labeler
Huons Co., Ltd.
Dosage form
Injection
Route
Subarachnoid
Marketing category
ANDA · ANDA212822
Marketed since
December 30, 2019
Listing expires
December 31, 2026
Pharmacologic class
Amide Local Anesthetic

Active ingredients

Uses, dosage, side effects and warnings for Bupivacaine Hydrochloride →

Package NDC codes (1)

Package NDCDescriptionSince
73293-0002-250 AMPULE in 1 PACKAGE (73293-0002-2) / 2 mL in 1 AMPULE (73293-0002-1)Dec 30, 2019

Recalls mentioning this NDC

Other Bupivacaine Hydrochloride products