Package 61314-016-01

Brand: proparacaine hydrochloride

Generic: proparacaine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 61314-016-01
Digits Only 6131401601
Product NDC 61314-016
Product ID 61314-016_ca203740-1e54-4289-9a1f-f2086fec4f46
Description

1 BOTTLE in 1 CARTON (61314-016-01) / 15 mL in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 2000-06-05
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": "ca203740-1e54-4289-9a1f-f2086fec4f46", "openfda": {"upc": ["0361314016010"], "unii": ["U96OL57GOY"], "rxcui": ["1191013"], "spl_set_id": ["447a2a64-0507-4fe8-bb44-cc36c3916151"], "manufacturer_name": ["Sandoz Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (61314-016-01)  / 15 mL in 1 BOTTLE", "package_ndc": "61314-016-01", "marketing_start_date": "20000605"}], "brand_name": "Proparacaine Hydrochloride", "product_id": "61314-016_ca203740-1e54-4289-9a1f-f2086fec4f46", "dosage_form": "SOLUTION/ DROPS", "pharm_class": ["Local Anesthesia [PE]", "Local Anesthetic [EPC]"], "product_ndc": "61314-016", "generic_name": "Proparacaine Hydrochloride", "labeler_name": "Sandoz Inc.", "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"}