bupivacaine hydrochloride

Generic: bupivacaine hydrochloride

Labeler: huons co., ltd.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name bupivacaine hydrochloride
Generic Name bupivacaine hydrochloride
Labeler huons co., ltd.
Dosage Form INJECTION
Routes
SUBARACHNOID
Active Ingredients

bupivacaine hydrochloride 7.5 mg/mL

Manufacturer
Huons Co., Ltd.

Identifiers & Regulatory

Product NDC 73293-0002
Product ID 73293-0002_2e641a0d-4d42-e7cd-e063-6394a90a47d4
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA212822
Listing Expiration 2026-12-31
Marketing Start 2019-12-30

Pharmacologic Class

Classes
amide local anesthetic [epc] amides [cs] local anesthesia [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 732930002
Hyphenated Format 73293-0002

Supplemental Identifiers

RxCUI
1724784
UPC
0373293000218
UNII
7TQO7W3VT8

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name bupivacaine hydrochloride (source: ndc)
Generic Name bupivacaine hydrochloride (source: ndc)
Application Number ANDA212822 (source: ndc)
Routes
SUBARACHNOID
source: ndc

Resolved Composition

Strengths
  • 7.5 mg/mL
source: ndc
Packaging
  • 50 AMPULE in 1 PACKAGE (73293-0002-2) / 2 mL in 1 AMPULE (73293-0002-1)
source: ndc

Packages (1)

Ingredients (1)

bupivacaine hydrochloride (7.5 mg/mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["SUBARACHNOID"], "spl_id": "2e641a0d-4d42-e7cd-e063-6394a90a47d4", "openfda": {"upc": ["0373293000218"], "unii": ["7TQO7W3VT8"], "rxcui": ["1724784"], "spl_set_id": ["2dc693df-3218-4a90-b3f7-21e80966a851"], "manufacturer_name": ["Huons Co., Ltd."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "50 AMPULE in 1 PACKAGE (73293-0002-2)  / 2 mL in 1 AMPULE (73293-0002-1)", "package_ndc": "73293-0002-2", "marketing_start_date": "20191230"}], "brand_name": "Bupivacaine Hydrochloride", "product_id": "73293-0002_2e641a0d-4d42-e7cd-e063-6394a90a47d4", "dosage_form": "INJECTION", "pharm_class": ["Amide Local Anesthetic [EPC]", "Amides [CS]", "Local Anesthesia [PE]"], "product_ndc": "73293-0002", "generic_name": "Bupivacaine hydrochloride", "labeler_name": "Huons Co., Ltd.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Bupivacaine Hydrochloride", "active_ingredients": [{"name": "BUPIVACAINE HYDROCHLORIDE", "strength": "7.5 mg/mL"}], "application_number": "ANDA212822", "marketing_category": "ANDA", "marketing_start_date": "20191230", "listing_expiration_date": "20261231"}