benzonatate

Generic: benzonatate

Labeler: pharmasource meds, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name benzonatate
Generic Name benzonatate
Labeler pharmasource meds, llc
Dosage Form CAPSULE
Routes
ORAL
Active Ingredients

benzonatate 200 mg/1

Manufacturer
Pharmasource Meds, LLC

Identifiers & Regulatory

Product NDC 82982-031
Product ID 82982-031_198c9eae-8e04-6548-e063-6394a90a5f50
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA206948
Marketing Start 2023-02-28
Marketing End 2026-03-31

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 82982031
Hyphenated Format 82982-031

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 ANDA206948 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 200 mg/1
source: ndc
Packaging
  • 30 CAPSULE in 1 BOTTLE (82982-031-30)
source: ndc

Packages (1)

82982-031-30 30 CAPSULE in 1 BOTTLE (82982-031-30)

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": "198c9eae-8e04-6548-e063-6394a90a5f50", "openfda": {"nui": ["N0000009010", "N0000175796"], "unii": ["5P4DHS6ENR"], "rxcui": ["283417"], "spl_set_id": ["f5c6b823-7a3c-6964-e053-2a95a90a737e"], "pharm_class_pe": ["Decreased Tracheobronchial Stretch Receptor Activity [PE]"], "pharm_class_epc": ["Non-narcotic Antitussive [EPC]"], "manufacturer_name": ["Pharmasource Meds, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE in 1 BOTTLE (82982-031-30)", "package_ndc": "82982-031-30", "marketing_end_date": "20260331", "marketing_start_date": "20230228"}], "brand_name": "Benzonatate", "product_id": "82982-031_198c9eae-8e04-6548-e063-6394a90a5f50", "dosage_form": "CAPSULE", "pharm_class": ["Decreased Tracheobronchial Stretch Receptor Activity [PE]", "Non-narcotic Antitussive [EPC]"], "product_ndc": "82982-031", "generic_name": "Benzonatate", "labeler_name": "Pharmasource Meds, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Benzonatate", "active_ingredients": [{"name": "BENZONATATE", "strength": "200 mg/1"}], "application_number": "ANDA206948", "marketing_category": "ANDA", "marketing_end_date": "20260331", "marketing_start_date": "20230228"}