benzonatate

Generic: benzonatate

Labeler: redpharm drug, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name benzonatate
Generic Name benzonatate
Labeler redpharm drug, inc.
Dosage Form CAPSULE
Routes
ORAL
Active Ingredients

benzonatate 200 mg/1

Manufacturer
RedPharm Drug, Inc.

Identifiers & Regulatory

Product NDC 67296-1751
Product ID 67296-1751_3252d7f4-3dc9-819c-e063-6294a90a9fa1
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA206948
Listing Expiration 2026-12-31
Marketing Start 2020-01-01

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 672961751
Hyphenated Format 67296-1751

Supplemental Identifiers

RxCUI
283417
UPC
0342806714010 0367296175134
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
  • 200 mg/1
source: ndc
Packaging
  • 30 CAPSULE in 1 BOTTLE (67296-1751-3)
  • 15 CAPSULE in 1 BOTTLE (67296-1751-5)
source: ndc

Packages (2)

67296-1751-3 30 CAPSULE in 1 BOTTLE (67296-1751-3) 67296-1751-5 15 CAPSULE in 1 BOTTLE (67296-1751-5)

Ingredients (1)

benzonatate (200 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": "3252d7f4-3dc9-819c-e063-6294a90a9fa1", "openfda": {"nui": ["N0000009010", "N0000175796"], "upc": ["0342806714010", "0367296175134"], "unii": ["5P4DHS6ENR"], "rxcui": ["283417"], "spl_set_id": ["a2f6acff-70ff-79f1-e053-2a95a90a6005"], "pharm_class_pe": ["Decreased Tracheobronchial Stretch Receptor Activity [PE]"], "pharm_class_epc": ["Non-narcotic Antitussive [EPC]"], "manufacturer_name": ["RedPharm Drug, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE in 1 BOTTLE (67296-1751-3)", "package_ndc": "67296-1751-3", "marketing_start_date": "20200101"}, {"sample": false, "description": "15 CAPSULE in 1 BOTTLE (67296-1751-5)", "package_ndc": "67296-1751-5", "marketing_start_date": "20200101"}], "brand_name": "Benzonatate", "product_id": "67296-1751_3252d7f4-3dc9-819c-e063-6294a90a9fa1", "dosage_form": "CAPSULE", "pharm_class": ["Decreased Tracheobronchial Stretch Receptor Activity [PE]", "Non-narcotic Antitussive [EPC]"], "product_ndc": "67296-1751", "generic_name": "Benzonatate", "labeler_name": "RedPharm Drug, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Benzonatate", "active_ingredients": [{"name": "BENZONATATE", "strength": "200 mg/1"}], "application_number": "ANDA206948", "marketing_category": "ANDA", "marketing_start_date": "20200101", "listing_expiration_date": "20261231"}