bupivacaine hydrochloride
Generic: bupivacaine hydrochloride
Labeler: hospira, inc.Drug Facts
Product Profile
Brand Name
bupivacaine hydrochloride
Generic Name
bupivacaine hydrochloride
Labeler
hospira, inc.
Dosage Form
INJECTION, SOLUTION
Routes
Active Ingredients
bupivacaine hydrochloride 5 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
0409-1163
Product ID
0409-1163_6e442bfd-d3da-4913-8585-ce3485644364
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA070597
Listing Expiration
2027-12-31
Marketing Start
2005-03-31
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
04091163
Hyphenated Format
0409-1163
Supplemental Identifiers
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
ANDA070597 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 5 mg/mL
Packaging
- 25 VIAL, MULTI-DOSE in 1 TRAY (0409-1163-01) / 50 mL in 1 VIAL, MULTI-DOSE (0409-1163-18)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["PERINEURAL"], "spl_id": "6e442bfd-d3da-4913-8585-ce3485644364", "openfda": {"unii": ["7TQO7W3VT8", "30Q7KI53AK"], "spl_set_id": ["02a845c3-4521-4926-e397-25ab536e7cf6"], "manufacturer_name": ["Hospira, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL, MULTI-DOSE in 1 TRAY (0409-1163-01) / 50 mL in 1 VIAL, MULTI-DOSE (0409-1163-18)", "package_ndc": "0409-1163-01", "marketing_start_date": "20050331"}], "brand_name": "Bupivacaine Hydrochloride", "product_id": "0409-1163_6e442bfd-d3da-4913-8585-ce3485644364", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Amide Local Anesthetic [EPC]", "Amides [CS]", "Local Anesthesia [PE]"], "product_ndc": "0409-1163", "generic_name": "BUPIVACAINE HYDROCHLORIDE", "labeler_name": "Hospira, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Bupivacaine Hydrochloride", "active_ingredients": [{"name": "BUPIVACAINE HYDROCHLORIDE", "strength": "5 mg/mL"}], "application_number": "ANDA070597", "marketing_category": "ANDA", "marketing_start_date": "20050331", "listing_expiration_date": "20271231"}