benzonatate
Generic: benzonatate
Labeler: proficient rx lpDrug Facts
Product Profile
Brand Name
benzonatate
Generic Name
benzonatate
Labeler
proficient rx lp
Dosage Form
CAPSULE
Routes
Active Ingredients
benzonatate 200 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
71205-673
Product ID
71205-673_8dcaeabf-e7da-4e0c-b6db-0bd425d6506e
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
71205673
Hyphenated Format
71205-673
Supplemental Identifiers
RxCUI
UPC
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
- 6 CAPSULE in 1 BOTTLE (71205-673-06)
- 10 CAPSULE in 1 BOTTLE (71205-673-10)
- 14 CAPSULE in 1 BOTTLE (71205-673-14)
- 15 CAPSULE in 1 BOTTLE (71205-673-15)
- 20 CAPSULE in 1 BOTTLE (71205-673-20)
- 21 CAPSULE in 1 BOTTLE (71205-673-21)
- 30 CAPSULE in 1 BOTTLE (71205-673-30)
- 60 CAPSULE in 1 BOTTLE (71205-673-60)
- 90 CAPSULE in 1 BOTTLE (71205-673-90)
Packages (9)
71205-673-06
6 CAPSULE in 1 BOTTLE (71205-673-06)
71205-673-10
10 CAPSULE in 1 BOTTLE (71205-673-10)
71205-673-14
14 CAPSULE in 1 BOTTLE (71205-673-14)
71205-673-15
15 CAPSULE in 1 BOTTLE (71205-673-15)
71205-673-20
20 CAPSULE in 1 BOTTLE (71205-673-20)
71205-673-21
21 CAPSULE in 1 BOTTLE (71205-673-21)
71205-673-30
30 CAPSULE in 1 BOTTLE (71205-673-30)
71205-673-60
60 CAPSULE in 1 BOTTLE (71205-673-60)
71205-673-90
90 CAPSULE in 1 BOTTLE (71205-673-90)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "8dcaeabf-e7da-4e0c-b6db-0bd425d6506e", "openfda": {"nui": ["N0000009010", "N0000175796"], "upc": ["0371205673307"], "unii": ["5P4DHS6ENR"], "rxcui": ["283417"], "spl_set_id": ["8dcaeabf-e7da-4e0c-b6db-0bd425d6506e"], "pharm_class_pe": ["Decreased Tracheobronchial Stretch Receptor Activity [PE]"], "pharm_class_epc": ["Non-narcotic Antitussive [EPC]"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "6 CAPSULE in 1 BOTTLE (71205-673-06)", "package_ndc": "71205-673-06", "marketing_start_date": "20220701"}, {"sample": false, "description": "10 CAPSULE in 1 BOTTLE (71205-673-10)", "package_ndc": "71205-673-10", "marketing_start_date": "20220701"}, {"sample": false, "description": "14 CAPSULE in 1 BOTTLE (71205-673-14)", "package_ndc": "71205-673-14", "marketing_start_date": "20220701"}, {"sample": false, "description": "15 CAPSULE in 1 BOTTLE (71205-673-15)", "package_ndc": "71205-673-15", "marketing_start_date": "20220701"}, {"sample": false, "description": "20 CAPSULE in 1 BOTTLE (71205-673-20)", "package_ndc": "71205-673-20", "marketing_start_date": "20220701"}, {"sample": false, "description": "21 CAPSULE in 1 BOTTLE (71205-673-21)", "package_ndc": "71205-673-21", "marketing_start_date": "20220701"}, {"sample": false, "description": "30 CAPSULE in 1 BOTTLE (71205-673-30)", "package_ndc": "71205-673-30", "marketing_start_date": "20220701"}, {"sample": false, "description": "60 CAPSULE in 1 BOTTLE (71205-673-60)", "package_ndc": "71205-673-60", "marketing_start_date": "20220701"}, {"sample": false, "description": "90 CAPSULE in 1 BOTTLE (71205-673-90)", "package_ndc": "71205-673-90", "marketing_start_date": "20220701"}], "brand_name": "Benzonatate", "product_id": "71205-673_8dcaeabf-e7da-4e0c-b6db-0bd425d6506e", "dosage_form": "CAPSULE", "pharm_class": ["Decreased Tracheobronchial Stretch Receptor Activity [PE]", "Non-narcotic Antitussive [EPC]"], "product_ndc": "71205-673", "generic_name": "Benzonatate", "labeler_name": "Proficient Rx LP", "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"}