benzonatate

Generic: benzonatate

Labeler: heritage pharmaceuticals inc. d/b/a avet pharmaceuticals inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name benzonatate
Generic Name benzonatate
Labeler heritage pharmaceuticals inc. d/b/a avet pharmaceuticals inc.
Dosage Form CAPSULE, LIQUID FILLED
Routes
ORAL
Active Ingredients

benzonatate 200 mg/1

Manufacturer
Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.

Identifiers & Regulatory

Product NDC 23155-899
Product ID 23155-899_0421e0c9-c73e-4eb4-a0cf-c67241a4749e
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA040682
Listing Expiration 2026-12-31
Marketing Start 2024-09-29

Pharmacologic Class

Established (EPC)
non-narcotic antitussive [epc]
Physiologic Effect
decreased tracheobronchial stretch receptor activity [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 23155899
Hyphenated Format 23155-899

Supplemental Identifiers

RxCUI
197397 283417
UNII
5P4DHS6ENR
NUI
N0000009010 N0000175796

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 benzonatate (source: ndc)
Generic Name benzonatate (source: ndc)
Application Number ANDA040682 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 200 mg/1
source: ndc
Packaging
  • 100 CAPSULE, LIQUID FILLED in 1 BOTTLE (23155-899-01)
  • 500 CAPSULE, LIQUID FILLED in 1 BOTTLE (23155-899-05)
source: ndc

Packages (2)

23155-899-01 100 CAPSULE, LIQUID FILLED in 1 BOTTLE (23155-899-01) 23155-899-05 500 CAPSULE, LIQUID FILLED in 1 BOTTLE (23155-899-05)

Ingredients (1)

benzonatate (200 mg/1)

Linked Drug Pages (1)

Benzonatate ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "0421e0c9-c73e-4eb4-a0cf-c67241a4749e", "openfda": {"nui": ["N0000009010", "N0000175796"], "unii": ["5P4DHS6ENR"], "rxcui": ["197397", "283417"], "spl_set_id": ["f32014c7-bc0c-4edb-b591-7baa6664d74b"], "pharm_class_pe": ["Decreased Tracheobronchial Stretch Receptor Activity [PE]"], "pharm_class_epc": ["Non-narcotic Antitussive [EPC]"], "manufacturer_name": ["Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE, LIQUID FILLED in 1 BOTTLE (23155-899-01)", "package_ndc": "23155-899-01", "marketing_start_date": "20240929"}, {"sample": false, "description": "500 CAPSULE, LIQUID FILLED in 1 BOTTLE (23155-899-05)", "package_ndc": "23155-899-05", "marketing_start_date": "20240929"}], "brand_name": "Benzonatate", "product_id": "23155-899_0421e0c9-c73e-4eb4-a0cf-c67241a4749e", "dosage_form": "CAPSULE, LIQUID FILLED", "pharm_class": ["Decreased Tracheobronchial Stretch Receptor Activity [PE]", "Non-narcotic Antitussive [EPC]"], "product_ndc": "23155-899", "generic_name": "Benzonatate", "labeler_name": "Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Benzonatate", "active_ingredients": [{"name": "BENZONATATE", "strength": "200 mg/1"}], "application_number": "ANDA040682", "marketing_category": "ANDA", "marketing_start_date": "20240929", "listing_expiration_date": "20261231"}