benzonatate

Generic: benzonatate

Labeler: direct_rx
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name benzonatate
Generic Name benzonatate
Labeler direct_rx
Dosage Form CAPSULE
Routes
ORAL
Active Ingredients

benzonatate 200 mg/1

Manufacturer
Direct_rx

Identifiers & Regulatory

Product NDC 72189-606
Product ID 72189-606_4b97132d-ac90-381e-e063-6294a90a615e
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA211518
Listing Expiration 2027-12-31
Marketing Start 2025-01-09

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 72189606
Hyphenated Format 72189-606

Supplemental Identifiers

RxCUI
283417
UNII
5P4DHS6ENR
NUI
N0000009010 N0000175796

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 ANDA211518 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 200 mg/1
source: ndc
Packaging
  • 20 CAPSULE in 1 BOTTLE (72189-606-20)
  • 30 CAPSULE in 1 BOTTLE (72189-606-30)
source: ndc

Packages (2)

72189-606-20 20 CAPSULE in 1 BOTTLE (72189-606-20) 72189-606-30 30 CAPSULE in 1 BOTTLE (72189-606-30)

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": "4b97132d-ac90-381e-e063-6294a90a615e", "openfda": {"nui": ["N0000009010", "N0000175796"], "unii": ["5P4DHS6ENR"], "rxcui": ["283417"], "spl_set_id": ["2b4b22e9-a03d-fb8f-e063-6394a90a8747"], "pharm_class_pe": ["Decreased Tracheobronchial Stretch Receptor Activity [PE]"], "pharm_class_epc": ["Non-narcotic Antitussive [EPC]"], "manufacturer_name": ["Direct_rx"]}, "finished": true, "packaging": [{"sample": false, "description": "20 CAPSULE in 1 BOTTLE (72189-606-20)", "package_ndc": "72189-606-20", "marketing_start_date": "20250109"}, {"sample": false, "description": "30 CAPSULE in 1 BOTTLE (72189-606-30)", "package_ndc": "72189-606-30", "marketing_start_date": "20250109"}], "brand_name": "Benzonatate", "product_id": "72189-606_4b97132d-ac90-381e-e063-6294a90a615e", "dosage_form": "CAPSULE", "pharm_class": ["Decreased Tracheobronchial Stretch Receptor Activity [PE]", "Non-narcotic Antitussive [EPC]"], "product_ndc": "72189-606", "generic_name": "Benzonatate", "labeler_name": "Direct_rx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Benzonatate", "active_ingredients": [{"name": "BENZONATATE", "strength": "200 mg/1"}], "application_number": "ANDA211518", "marketing_category": "ANDA", "marketing_start_date": "20250109", "listing_expiration_date": "20271231"}