benzonatate
Generic: benzonatate
Labeler: coupler llcDrug Facts
Product Profile
Brand Name
benzonatate
Generic Name
benzonatate
Labeler
coupler llc
Dosage Form
CAPSULE
Routes
Active Ingredients
benzonatate 100 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
67046-1629
Product ID
67046-1629_463d6418-04ce-05f0-e063-6294a90ac910
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA040627
Listing Expiration
2026-12-31
Marketing Start
2025-12-18
Pharmacologic Class
Established (EPC)
Physiologic Effect
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
670461629
Hyphenated Format
67046-1629
Supplemental Identifiers
RxCUI
UNII
NUI
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
ANDA040627 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 100 mg/1
Packaging
- 30 CAPSULE in 1 BLISTER PACK (67046-1629-3)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "463d6418-04ce-05f0-e063-6294a90ac910", "openfda": {"nui": ["N0000009010", "N0000175796"], "unii": ["5P4DHS6ENR"], "rxcui": ["197397"], "spl_set_id": ["463d5cff-3cd6-58fc-e063-6394a90a996b"], "pharm_class_pe": ["Decreased Tracheobronchial Stretch Receptor Activity [PE]"], "pharm_class_epc": ["Non-narcotic Antitussive [EPC]"], "manufacturer_name": ["Coupler LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE in 1 BLISTER PACK (67046-1629-3)", "package_ndc": "67046-1629-3", "marketing_start_date": "20251218"}], "brand_name": "BENZONATATE", "product_id": "67046-1629_463d6418-04ce-05f0-e063-6294a90ac910", "dosage_form": "CAPSULE", "pharm_class": ["Decreased Tracheobronchial Stretch Receptor Activity [PE]", "Non-narcotic Antitussive [EPC]"], "product_ndc": "67046-1629", "generic_name": "BENZONATATE", "labeler_name": "Coupler LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "BENZONATATE", "active_ingredients": [{"name": "BENZONATATE", "strength": "100 mg/1"}], "application_number": "ANDA040627", "marketing_category": "ANDA", "marketing_start_date": "20251218", "listing_expiration_date": "20261231"}