Package 85766-056-15

Brand: proparacaine hydrochloride

Generic: proparacaine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 85766-056-15
Digits Only 8576605615
Product NDC 85766-056
Description

1 BOTTLE in 1 CARTON (85766-056-15) / 15 mL in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 2025-08-22
Brand proparacaine hydrochloride
Generic proparacaine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["OPHTHALMIC"], "spl_id": "3ceea62b-dfaa-17a6-e063-6394a90aaa08", "openfda": {"unii": ["U96OL57GOY"], "rxcui": ["1191013"], "spl_set_id": ["1d257859-cd1d-485f-a4d5-dbb33c1ec197"], "manufacturer_name": ["Sportpharm, Inc. dba Sportpharm"]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (85766-056-15)  / 15 mL in 1 BOTTLE", "package_ndc": "85766-056-15", "marketing_start_date": "20250822"}], "brand_name": "Proparacaine Hydrochloride", "product_id": "85766-056_3ceea62b-dfaa-17a6-e063-6394a90aaa08", "dosage_form": "SOLUTION/ DROPS", "pharm_class": ["Local Anesthesia [PE]", "Local Anesthetic [EPC]"], "product_ndc": "85766-056", "generic_name": "Proparacaine Hydrochloride", "labeler_name": "Sportpharm, Inc. dba Sportpharm", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Proparacaine Hydrochloride", "active_ingredients": [{"name": "PROPARACAINE HYDROCHLORIDE", "strength": "5 mg/mL"}], "application_number": "ANDA080027", "marketing_category": "ANDA", "marketing_start_date": "20000605", "listing_expiration_date": "20261231"}