mepivacaine
Generic: mepivacaine hydrochloride
Labeler: ndc, inc.Drug Facts
Product Profile
Brand Name
mepivacaine
Generic Name
mepivacaine hydrochloride
Labeler
ndc, inc.
Dosage Form
INJECTION, SOLUTION
Routes
Active Ingredients
mepivacaine hydrochloride 30 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
43128-005
Product ID
43128-005_d65ce2b4-0c6a-4edd-bb95-c7f463db8dd4
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA088387
Listing Expiration
2026-12-31
Marketing Start
2015-04-10
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
43128005
Hyphenated Format
43128-005
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
mepivacaine (source: ndc)
Generic Name
mepivacaine hydrochloride (source: ndc)
Application Number
ANDA088387 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 30 mg/mL
Packaging
- 50 CARTRIDGE in 1 CARTON (43128-005-35) / 1.7 mL in 1 CARTRIDGE
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["SUBMUCOSAL"], "spl_id": "d65ce2b4-0c6a-4edd-bb95-c7f463db8dd4", "openfda": {"unii": ["4VFX2L7EM5"], "rxcui": ["1305263"], "spl_set_id": ["042010fb-7161-4336-b91f-5a25839ee644"], "manufacturer_name": ["NDC, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "50 CARTRIDGE in 1 CARTON (43128-005-35) / 1.7 mL in 1 CARTRIDGE", "package_ndc": "43128-005-35", "marketing_start_date": "20150410"}], "brand_name": "Mepivacaine", "product_id": "43128-005_d65ce2b4-0c6a-4edd-bb95-c7f463db8dd4", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Amide Local Anesthetic [EPC]", "Amides [CS]", "Local Anesthesia [PE]"], "product_ndc": "43128-005", "generic_name": "Mepivacaine Hydrochloride", "labeler_name": "NDC, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Mepivacaine", "active_ingredients": [{"name": "MEPIVACAINE HYDROCHLORIDE", "strength": "30 mg/mL"}], "application_number": "ANDA088387", "marketing_category": "ANDA", "marketing_start_date": "20150410", "listing_expiration_date": "20261231"}