Package 70069-601-01

Brand: proparacaine hydrochloride

Generic: proparacaine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70069-601-01
Digits Only 7006960101
Product NDC 70069-601
Product ID 70069-601_abb9ea27-1536-41b3-b84e-839796fdf710
Description

1 BOTTLE in 1 CARTON (70069-601-01) / 15 mL in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 2024-10-10
Brand proparacaine hydrochloride
Generic proparacaine hydrochloride
Sample Package No

Linked Drug Pages (1)

Proparacaine Hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["OPHTHALMIC"], "spl_id": "abb9ea27-1536-41b3-b84e-839796fdf710", "openfda": {"upc": ["0370069601013"], "unii": ["U96OL57GOY"], "rxcui": ["1191013"], "spl_set_id": ["968a6e4e-814f-41f8-ae22-aa5a82179a6c"], "manufacturer_name": ["Somerset Therapeutics, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (70069-601-01)  / 15 mL in 1 BOTTLE", "package_ndc": "70069-601-01", "marketing_start_date": "20241010"}], "brand_name": "Proparacaine Hydrochloride", "product_id": "70069-601_abb9ea27-1536-41b3-b84e-839796fdf710", "dosage_form": "SOLUTION/ DROPS", "pharm_class": ["Local Anesthesia [PE]", "Local Anesthetic [EPC]"], "product_ndc": "70069-601", "generic_name": "Proparacaine Hydrochloride", "labeler_name": "Somerset Therapeutics, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Proparacaine Hydrochloride", "active_ingredients": [{"name": "PROPARACAINE HYDROCHLORIDE", "strength": "5 mg/mL"}], "application_number": "ANDA215816", "marketing_category": "ANDA", "marketing_start_date": "20241010", "listing_expiration_date": "20261231"}