benzonatate

Generic: benzonatate

Labeler: proficient rx lp
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name benzonatate
Generic Name benzonatate
Labeler proficient rx lp
Dosage Form CAPSULE
Routes
ORAL
Active Ingredients

benzonatate 100 mg/1

Manufacturer
Proficient Rx LP

Identifiers & Regulatory

Product NDC 71205-632
Product ID 71205-632_a449d609-2233-477e-bdb7-df2c84a1b495
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA206948
Listing Expiration 2026-12-31
Marketing Start 2018-12-21

Pharmacologic Class

Established (EPC)
non-narcotic antitussive [epc]
Physiologic Effect
decreased tracheobronchial stretch receptor activity [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 71205632
Hyphenated Format 71205-632

Supplemental Identifiers

RxCUI
197397
UPC
0371205632205
UNII
5P4DHS6ENR
NUI
N0000009010 N0000175796

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 ANDA206948 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 100 mg/1
source: ndc
Packaging
  • 10 CAPSULE in 1 BOTTLE (71205-632-10)
  • 15 CAPSULE in 1 BOTTLE (71205-632-15)
  • 20 CAPSULE in 1 BOTTLE (71205-632-20)
  • 21 CAPSULE in 1 BOTTLE (71205-632-21)
  • 30 CAPSULE in 1 BOTTLE (71205-632-30)
  • 60 CAPSULE in 1 BOTTLE (71205-632-60)
  • 90 CAPSULE in 1 BOTTLE (71205-632-90)
source: ndc

Packages (7)

71205-632-10 10 CAPSULE in 1 BOTTLE (71205-632-10) 71205-632-15 15 CAPSULE in 1 BOTTLE (71205-632-15) 71205-632-20 20 CAPSULE in 1 BOTTLE (71205-632-20) 71205-632-21 21 CAPSULE in 1 BOTTLE (71205-632-21) 71205-632-30 30 CAPSULE in 1 BOTTLE (71205-632-30) 71205-632-60 60 CAPSULE in 1 BOTTLE (71205-632-60) 71205-632-90 90 CAPSULE in 1 BOTTLE (71205-632-90)

Ingredients (1)

benzonatate (100 mg/1)

Linked Drug Pages (1)

Benzonatate ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "a449d609-2233-477e-bdb7-df2c84a1b495", "openfda": {"nui": ["N0000009010", "N0000175796"], "upc": ["0371205632205"], "unii": ["5P4DHS6ENR"], "rxcui": ["197397"], "spl_set_id": ["46b4f05c-9261-42fc-a016-c99eebab5646"], "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": "10 CAPSULE in 1 BOTTLE (71205-632-10)", "package_ndc": "71205-632-10", "marketing_start_date": "20220119"}, {"sample": false, "description": "15 CAPSULE in 1 BOTTLE (71205-632-15)", "package_ndc": "71205-632-15", "marketing_start_date": "20220119"}, {"sample": false, "description": "20 CAPSULE in 1 BOTTLE (71205-632-20)", "package_ndc": "71205-632-20", "marketing_start_date": "20220119"}, {"sample": false, "description": "21 CAPSULE in 1 BOTTLE (71205-632-21)", "package_ndc": "71205-632-21", "marketing_start_date": "20220119"}, {"sample": false, "description": "30 CAPSULE in 1 BOTTLE (71205-632-30)", "package_ndc": "71205-632-30", "marketing_start_date": "20220119"}, {"sample": false, "description": "60 CAPSULE in 1 BOTTLE (71205-632-60)", "package_ndc": "71205-632-60", "marketing_start_date": "20220119"}, {"sample": false, "description": "90 CAPSULE in 1 BOTTLE (71205-632-90)", "package_ndc": "71205-632-90", "marketing_start_date": "20220119"}], "brand_name": "Benzonatate", "product_id": "71205-632_a449d609-2233-477e-bdb7-df2c84a1b495", "dosage_form": "CAPSULE", "pharm_class": ["Decreased Tracheobronchial Stretch Receptor Activity [PE]", "Non-narcotic Antitussive [EPC]"], "product_ndc": "71205-632", "generic_name": "Benzonatate", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Benzonatate", "active_ingredients": [{"name": "BENZONATATE", "strength": "100 mg/1"}], "application_number": "ANDA206948", "marketing_category": "ANDA", "marketing_start_date": "20181221", "listing_expiration_date": "20261231"}