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
67046-1484
Product ID
67046-1484_2ce03083-d6c3-8a00-e063-6294a90aba68
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA081297
Listing Expiration
2026-12-31
Marketing Start
2025-01-29
Pharmacologic Class
Established (EPC)
Physiologic Effect
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
670461484
Hyphenated Format
67046-1484
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
ANDA081297 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 100 mg/1
Packaging
- 30 CAPSULE in 1 BLISTER PACK (67046-1484-3)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2ce03083-d6c3-8a00-e063-6294a90aba68", "openfda": {"nui": ["N0000009010", "N0000175796"], "unii": ["5P4DHS6ENR"], "rxcui": ["197397"], "spl_set_id": ["2ce035ff-42cb-d8ef-e063-6294a90a0c06"], "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 (67046-1484-3)", "package_ndc": "67046-1484-3", "marketing_start_date": "20250129"}], "brand_name": "Benzonatate", "product_id": "67046-1484_2ce03083-d6c3-8a00-e063-6294a90aba68", "dosage_form": "CAPSULE", "pharm_class": ["Decreased Tracheobronchial Stretch Receptor Activity [PE]", "Non-narcotic Antitussive [EPC]"], "product_ndc": "67046-1484", "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": "ANDA081297", "marketing_category": "ANDA", "marketing_start_date": "20250129", "listing_expiration_date": "20261231"}