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
71335-0725
Product ID
71335-0725_1c471368-6338-4e1e-b93d-8fcb5022a1f5
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA040749
Listing Expiration
2026-12-31
Marketing Start
2017-03-22
Pharmacologic Class
Established (EPC)
Physiologic Effect
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
713350725
Hyphenated Format
71335-0725
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
ANDA040749 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 200 mg/1
Packaging
- 30 CAPSULE in 1 BOTTLE (71335-0725-1)
- 100 CAPSULE in 1 BOTTLE (71335-0725-2)
- 45 CAPSULE in 1 BOTTLE (71335-0725-3)
- 20 CAPSULE in 1 BOTTLE (71335-0725-4)
- 15 CAPSULE in 1 BOTTLE (71335-0725-5)
- 21 CAPSULE in 1 BOTTLE (71335-0725-6)
- 60 CAPSULE in 1 BOTTLE (71335-0725-7)
- 50 CAPSULE in 1 BOTTLE (71335-0725-8)
- 90 CAPSULE in 1 BOTTLE (71335-0725-9)
Packages (9)
71335-0725-1
30 CAPSULE in 1 BOTTLE (71335-0725-1)
71335-0725-2
100 CAPSULE in 1 BOTTLE (71335-0725-2)
71335-0725-3
45 CAPSULE in 1 BOTTLE (71335-0725-3)
71335-0725-4
20 CAPSULE in 1 BOTTLE (71335-0725-4)
71335-0725-5
15 CAPSULE in 1 BOTTLE (71335-0725-5)
71335-0725-6
21 CAPSULE in 1 BOTTLE (71335-0725-6)
71335-0725-7
60 CAPSULE in 1 BOTTLE (71335-0725-7)
71335-0725-8
50 CAPSULE in 1 BOTTLE (71335-0725-8)
71335-0725-9
90 CAPSULE in 1 BOTTLE (71335-0725-9)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "1c471368-6338-4e1e-b93d-8fcb5022a1f5", "openfda": {"nui": ["N0000009010", "N0000175796"], "unii": ["5P4DHS6ENR"], "rxcui": ["197397", "283417"], "spl_set_id": ["a788cb01-6dc3-4f28-aaa0-c23ac058c39a"], "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": "30 CAPSULE in 1 BOTTLE (71335-0725-1)", "package_ndc": "71335-0725-1", "marketing_start_date": "20180313"}, {"sample": false, "description": "100 CAPSULE in 1 BOTTLE (71335-0725-2)", "package_ndc": "71335-0725-2", "marketing_start_date": "20180313"}, {"sample": false, "description": "45 CAPSULE in 1 BOTTLE (71335-0725-3)", "package_ndc": "71335-0725-3", "marketing_start_date": "20180313"}, {"sample": false, "description": "20 CAPSULE in 1 BOTTLE (71335-0725-4)", "package_ndc": "71335-0725-4", "marketing_start_date": "20180313"}, {"sample": false, "description": "15 CAPSULE in 1 BOTTLE (71335-0725-5)", "package_ndc": "71335-0725-5", "marketing_start_date": "20180313"}, {"sample": false, "description": "21 CAPSULE in 1 BOTTLE (71335-0725-6)", "package_ndc": "71335-0725-6", "marketing_start_date": "20180313"}, {"sample": false, "description": "60 CAPSULE in 1 BOTTLE (71335-0725-7)", "package_ndc": "71335-0725-7", "marketing_start_date": "20180313"}, {"sample": false, "description": "50 CAPSULE in 1 BOTTLE (71335-0725-8)", "package_ndc": "71335-0725-8", "marketing_start_date": "20180313"}, {"sample": false, "description": "90 CAPSULE in 1 BOTTLE (71335-0725-9)", "package_ndc": "71335-0725-9", "marketing_start_date": "20180313"}], "brand_name": "benzonatate", "product_id": "71335-0725_1c471368-6338-4e1e-b93d-8fcb5022a1f5", "dosage_form": "CAPSULE", "pharm_class": ["Decreased Tracheobronchial Stretch Receptor Activity [PE]", "Non-narcotic Antitussive [EPC]"], "product_ndc": "71335-0725", "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": "ANDA040749", "marketing_category": "ANDA", "marketing_start_date": "20170322", "listing_expiration_date": "20261231"}