bupivacaine hydrochloride
Generic: bupivacaine hydrochloride
Labeler: hf acquisition co llc, dba healthfirstDrug Facts
Product Profile
Brand Name
bupivacaine hydrochloride
Generic Name
bupivacaine hydrochloride
Labeler
hf acquisition co llc, dba healthfirst
Dosage Form
INJECTION, SOLUTION
Routes
Active Ingredients
bupivacaine hydrochloride 5 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
51662-1396
Product ID
51662-1396_1b5824c7-c46a-48c6-e063-6394a90a22ce
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA070597
Listing Expiration
2026-12-31
Marketing Start
2019-10-16
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
516621396
Hyphenated Format
51662-1396
Supplemental Identifiers
RxCUI
UNII
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
- 50 mL in 1 VIAL, MULTI-DOSE (51662-1396-1)
- 25 POUCH in 1 CASE (51662-1396-3) / 1 mL in 1 POUCH (51662-1396-2)
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["PERINEURAL"], "spl_id": "1b5824c7-c46a-48c6-e063-6394a90a22ce", "openfda": {"unii": ["7TQO7W3VT8"], "rxcui": ["1012396", "1012404"], "spl_set_id": ["950d82b6-76a1-0c08-e053-2a95a90a3a92"], "manufacturer_name": ["HF Acquisition Co LLC, DBA HealthFirst"]}, "finished": true, "packaging": [{"sample": false, "description": "50 mL in 1 VIAL, MULTI-DOSE (51662-1396-1)", "package_ndc": "51662-1396-1", "marketing_start_date": "20191016"}, {"sample": false, "description": "25 POUCH in 1 CASE (51662-1396-3) / 1 mL in 1 POUCH (51662-1396-2)", "package_ndc": "51662-1396-3", "marketing_start_date": "20201027"}], "brand_name": "BUPIVACAINE HYDROCHLORIDE", "product_id": "51662-1396_1b5824c7-c46a-48c6-e063-6394a90a22ce", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Amide Local Anesthetic [EPC]", "Amides [CS]", "Local Anesthesia [PE]"], "product_ndc": "51662-1396", "generic_name": "BUPIVACAINE HYDROCHLORIDE", "labeler_name": "HF Acquisition Co LLC, DBA HealthFirst", "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": "20191016", "listing_expiration_date": "20261231"}