benzonatate
Generic: benzonatate
Labeler: major pharmaceuticals, inc.Drug Facts
Product Profile
Brand Name
benzonatate
Generic Name
benzonatate
Labeler
major pharmaceuticals, inc.
Dosage Form
CAPSULE
Routes
Active Ingredients
benzonatate 100 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
0904-6564
Product ID
0904-6564_2a1b6d7a-a9a2-4732-a803-01af654c0732
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA040597
Listing Expiration
2026-12-31
Marketing Start
2007-09-04
Pharmacologic Class
Established (EPC)
Physiologic Effect
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
09046564
Hyphenated Format
0904-6564
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
ANDA040597 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 100 mg/1
Packaging
- 100 CAPSULE in 1 BOTTLE (0904-6564-60)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2a1b6d7a-a9a2-4732-a803-01af654c0732", "openfda": {"nui": ["N0000009010", "N0000175796"], "unii": ["5P4DHS6ENR"], "rxcui": ["197397"], "spl_set_id": ["2256f7e4-b7e6-433f-941e-bf78ddcd55b2"], "pharm_class_pe": ["Decreased Tracheobronchial Stretch Receptor Activity [PE]"], "pharm_class_epc": ["Non-narcotic Antitussive [EPC]"], "manufacturer_name": ["Major Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (0904-6564-60)", "package_ndc": "0904-6564-60", "marketing_start_date": "20070904"}], "brand_name": "Benzonatate", "product_id": "0904-6564_2a1b6d7a-a9a2-4732-a803-01af654c0732", "dosage_form": "CAPSULE", "pharm_class": ["Decreased Tracheobronchial Stretch Receptor Activity [PE]", "Non-narcotic Antitussive [EPC]"], "product_ndc": "0904-6564", "generic_name": "Benzonatate", "labeler_name": "Major Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Benzonatate", "active_ingredients": [{"name": "BENZONATATE", "strength": "100 mg/1"}], "application_number": "ANDA040597", "marketing_category": "ANDA", "marketing_start_date": "20070904", "listing_expiration_date": "20261231"}