benzonatate
Generic: benzonatate
Labeler: bryant ranch prepackDrug Facts
Product Profile
Brand Name
benzonatate
Generic Name
benzonatate
Labeler
bryant ranch prepack
Dosage Form
CAPSULE
Routes
Active Ingredients
benzonatate 200 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
72162-1316
Product ID
72162-1316_01c4f415-1f2d-413b-8696-85aec7791fac
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA211518
Listing Expiration
2026-12-31
Marketing Start
2019-02-22
Pharmacologic Class
Established (EPC)
Physiologic Effect
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
721621316
Hyphenated Format
72162-1316
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
ANDA211518 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 200 mg/1
Packaging
- 100 CAPSULE in 1 BOTTLE (72162-1316-1)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "01c4f415-1f2d-413b-8696-85aec7791fac", "openfda": {"nui": ["N0000009010", "N0000175796"], "unii": ["5P4DHS6ENR"], "rxcui": ["283417"], "spl_set_id": ["da093b5e-83a7-467e-9716-bc5827a18c20"], "pharm_class_pe": ["Decreased Tracheobronchial Stretch Receptor Activity [PE]"], "pharm_class_epc": ["Non-narcotic Antitussive [EPC]"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (72162-1316-1)", "package_ndc": "72162-1316-1", "marketing_start_date": "20230829"}], "brand_name": "Benzonatate", "product_id": "72162-1316_01c4f415-1f2d-413b-8696-85aec7791fac", "dosage_form": "CAPSULE", "pharm_class": ["Decreased Tracheobronchial Stretch Receptor Activity [PE]", "Non-narcotic Antitussive [EPC]"], "product_ndc": "72162-1316", "generic_name": "Benzonatate", "labeler_name": "Bryant Ranch Prepack", "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": "20190222", "listing_expiration_date": "20261231"}