bupivacaine hydrochloride
Generic: bupivacaine hydrochloride
Labeler: meitheal pharmaceuticals incDrug Facts
Product Profile
Brand Name
bupivacaine hydrochloride
Generic Name
bupivacaine hydrochloride
Labeler
meitheal pharmaceuticals inc
Dosage Form
INJECTION, SOLUTION
Routes
Active Ingredients
bupivacaine hydrochloride 2.5 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
71288-723
Product ID
71288-723_0949c302-51ce-4fc9-8b99-1df94e693718
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA216039
Listing Expiration
2026-12-31
Marketing Start
2023-06-23
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
71288723
Hyphenated Format
71288-723
Supplemental Identifiers
RxCUI
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
ANDA216039 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 2.5 mg/mL
Packaging
- 1 VIAL, MULTI-DOSE in 1 CARTON (71288-723-52) / 50 mL in 1 VIAL, MULTI-DOSE
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INFILTRATION", "PERINEURAL"], "spl_id": "0949c302-51ce-4fc9-8b99-1df94e693718", "openfda": {"unii": ["7TQO7W3VT8"], "rxcui": ["1012396", "1012404"], "spl_set_id": ["fe340f98-a0f3-446e-b281-47fd91c1e537"], "manufacturer_name": ["Meitheal Pharmaceuticals Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, MULTI-DOSE in 1 CARTON (71288-723-52) / 50 mL in 1 VIAL, MULTI-DOSE", "package_ndc": "71288-723-52", "marketing_start_date": "20230623"}], "brand_name": "bupivacaine hydrochloride", "product_id": "71288-723_0949c302-51ce-4fc9-8b99-1df94e693718", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Amide Local Anesthetic [EPC]", "Amides [CS]", "Local Anesthesia [PE]"], "product_ndc": "71288-723", "generic_name": "bupivacaine hydrochloride", "labeler_name": "Meitheal Pharmaceuticals Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "bupivacaine hydrochloride", "active_ingredients": [{"name": "BUPIVACAINE HYDROCHLORIDE", "strength": "2.5 mg/mL"}], "application_number": "ANDA216039", "marketing_category": "ANDA", "marketing_start_date": "20230623", "listing_expiration_date": "20261231"}