carteolol hydrochloride (61314-238)

Drug Facts

Product Profile

Brand Name carteolol hydrochloride

Generic Name carteolol hydrochloride

Labeler sandoz inc

Dosage Form SOLUTION

Routes

OPHTHALMIC

Active Ingredients

carteolol hydrochloride 10 mg/mL

Manufacturer

Sandoz Inc

Identifiers & Regulatory

Product NDC 61314-238

Product ID 61314-238_c89793f0-318b-4481-8fc0-e9cb0dcc5244

Product Type HUMAN PRESCRIPTION DRUG

Marketing Category ANDA

Application Number ANDA075476

Listing Expiration 2026-12-31

Marketing Start 2000-01-05

Pharmacologic Class

Classes

adrenergic beta-antagonists [moa] beta-adrenergic blocker [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 61314238

Hyphenated Format 61314-238

Supplemental Identifiers

RxCUI

978573

UNII

4797W6I0T4

Packaging Origin

Original Packager

true

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 carteolol hydrochloride (source: ndc)

Generic Name carteolol hydrochloride (source: ndc)

Application Number ANDA075476 (source: ndc)

Routes

OPHTHALMIC

source: ndc

Resolved Composition

Strengths

10 mg/mL

source: ndc

Packaging

5 mL in 1 BOTTLE, PLASTIC (61314-238-05)
10 mL in 1 BOTTLE, PLASTIC (61314-238-10)
15 mL in 1 BOTTLE, PLASTIC (61314-238-15)

source: ndc

Packages (3)

61314-238-05 5 mL in 1 BOTTLE, PLASTIC (61314-238-05) 61314-238-10 10 mL in 1 BOTTLE, PLASTIC (61314-238-10) 61314-238-15 15 mL in 1 BOTTLE, PLASTIC (61314-238-15)

Ingredients (1)

carteolol hydrochloride (10 mg/mL)

Linked Drug Pages (1)

Carteolol Hydrochloride ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload

{"route": ["OPHTHALMIC"], "spl_id": "c89793f0-318b-4481-8fc0-e9cb0dcc5244", "openfda": {"unii": ["4797W6I0T4"], "rxcui": ["978573"], "spl_set_id": ["571fe550-399d-4296-835c-37aa1ab9b409"], "manufacturer_name": ["Sandoz Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "5 mL in 1 BOTTLE, PLASTIC (61314-238-05)", "package_ndc": "61314-238-05", "marketing_start_date": "20000105"}, {"sample": false, "description": "10 mL in 1 BOTTLE, PLASTIC (61314-238-10)", "package_ndc": "61314-238-10", "marketing_start_date": "20000105"}, {"sample": false, "description": "15 mL in 1 BOTTLE, PLASTIC (61314-238-15)", "package_ndc": "61314-238-15", "marketing_start_date": "20000105"}], "brand_name": "Carteolol Hydrochloride", "product_id": "61314-238_c89793f0-318b-4481-8fc0-e9cb0dcc5244", "dosage_form": "SOLUTION", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "61314-238", "generic_name": "Carteolol Hydrochloride", "labeler_name": "Sandoz Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Carteolol Hydrochloride", "active_ingredients": [{"name": "CARTEOLOL HYDROCHLORIDE", "strength": "10 mg/mL"}], "application_number": "ANDA075476", "marketing_category": "ANDA", "marketing_start_date": "20000105", "listing_expiration_date": "20261231"}