Package 84549-209-10

Brand: chloroprocaine hydrochloride

Generic: chloroprocaine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 84549-209-10
Digits Only 8454920910
Product NDC 84549-209
Description

20 mL in 1 VIAL (84549-209-10)

Marketing

Marketing Status
Marketed Since 2025-10-10
Brand chloroprocaine hydrochloride
Generic chloroprocaine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["EPIDURAL", "INFILTRATION", "INTRACAUDAL", "PERINEURAL"], "spl_id": "463ee055-62a2-9709-e063-6294a90aa7ed", "openfda": {"unii": ["LT7Z1YW11H"], "rxcui": ["1794184"], "spl_set_id": ["4305ab6b-6038-9daa-e063-6294a90a018e"], "manufacturer_name": ["ProPharma Distribution"]}, "finished": true, "packaging": [{"sample": false, "description": "20 mL in 1 VIAL (84549-209-10)", "package_ndc": "84549-209-10", "marketing_start_date": "20251010"}], "brand_name": "Chloroprocaine Hydrochloride", "product_id": "84549-209_463ee055-62a2-9709-e063-6294a90aa7ed", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Ester Local Anesthetic [EPC]", "Esters [CS]", "Local Anesthesia [PE]"], "product_ndc": "84549-209", "generic_name": "Chloroprocaine Hydrochloride", "labeler_name": "ProPharma Distribution", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Chloroprocaine Hydrochloride", "active_ingredients": [{"name": "CHLOROPROCAINE HYDROCHLORIDE", "strength": "20 mg/mL"}], "application_number": "ANDA040273", "marketing_category": "ANDA", "marketing_start_date": "19981101", "listing_expiration_date": "20261231"}