proparacaine hydrochloride
Generic: proparacaine hydrochloride
Labeler: sandoz inc.Drug Facts
Product Profile
Brand Name
proparacaine hydrochloride
Generic Name
proparacaine hydrochloride
Labeler
sandoz inc.
Dosage Form
SOLUTION/ DROPS
Routes
Active Ingredients
proparacaine hydrochloride 5 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
61314-016
Product ID
61314-016_ca203740-1e54-4289-9a1f-f2086fec4f46
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA080027
Listing Expiration
2026-12-31
Marketing Start
2000-06-05
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
61314016
Hyphenated Format
61314-016
Supplemental Identifiers
RxCUI
UPC
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
proparacaine hydrochloride (source: ndc)
Generic Name
proparacaine hydrochloride (source: ndc)
Application Number
ANDA080027 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 5 mg/mL
Packaging
- 1 BOTTLE in 1 CARTON (61314-016-01) / 15 mL in 1 BOTTLE
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
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"}