bupivacaine hydrochloride
Generic: bupivacaine hydrochloride
Labeler: huons co., ltd.Drug Facts
Product Profile
Brand Name
bupivacaine hydrochloride
Generic Name
bupivacaine hydrochloride
Labeler
huons co., ltd.
Dosage Form
INJECTION
Routes
Active Ingredients
bupivacaine hydrochloride 7.5 mg/mL
Manufacturer
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
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
732930002
Hyphenated Format
73293-0002
Supplemental Identifiers
RxCUI
UPC
UNII
Packaging Origin
Original Packager
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
source: ndc
Resolved Composition
Strengths
- 7.5 mg/mL
Packaging
- 50 AMPULE in 1 PACKAGE (73293-0002-2) / 2 mL in 1 AMPULE (73293-0002-1)
Packages (1)
Ingredients (1)
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"}