bupivicaine hydrochloride
Generic: bupivicaine hydrochloride
Labeler: hf acquisition co llc, dba healthfirstDrug Facts
Product Profile
Brand Name
bupivicaine hydrochloride
Generic Name
bupivicaine hydrochloride
Labeler
hf acquisition co llc, dba healthfirst
Dosage Form
INJECTION, SOLUTION
Routes
Active Ingredients
bupivacaine hydrochloride 2.5 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
51662-1456
Product ID
51662-1456_b107e2b0-091e-b326-e053-2a95a90aa253
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA070583
Listing Expiration
2026-12-31
Marketing Start
2019-12-12
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
516621456
Hyphenated Format
51662-1456
Supplemental Identifiers
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
bupivicaine hydrochloride (source: ndc)
Generic Name
bupivicaine hydrochloride (source: ndc)
Application Number
ANDA070583 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 2.5 mg/mL
Packaging
- 30 mL in 1 VIAL, SINGLE-DOSE (51662-1456-1)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["EPIDURAL", "INFILTRATION", "INTRACAUDAL", "PERINEURAL"], "spl_id": "b107e2b0-091e-b326-e053-2a95a90aa253", "openfda": {"unii": ["7TQO7W3VT8"], "spl_set_id": ["99857946-6084-1bbd-e053-2a95a90af58c"], "manufacturer_name": ["HF Acquisition Co LLC, DBA HealthFirst"]}, "finished": true, "packaging": [{"sample": false, "description": "30 mL in 1 VIAL, SINGLE-DOSE (51662-1456-1)", "package_ndc": "51662-1456-1", "marketing_start_date": "20191212"}], "brand_name": "BUPIVICAINE HYDROCHLORIDE", "product_id": "51662-1456_b107e2b0-091e-b326-e053-2a95a90aa253", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Amide Local Anesthetic [EPC]", "Amides [CS]", "Local Anesthesia [PE]"], "product_ndc": "51662-1456", "generic_name": "BUPIVICAINE HYDROCHLORIDE", "labeler_name": "HF Acquisition Co LLC, DBA HealthFirst", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "BUPIVICAINE HYDROCHLORIDE", "active_ingredients": [{"name": "BUPIVACAINE HYDROCHLORIDE", "strength": "2.5 mg/mL"}], "application_number": "ANDA070583", "marketing_category": "ANDA", "marketing_start_date": "20191212", "listing_expiration_date": "20261231"}