benzonatate

Generic: benzonatate

Labeler: camber pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name benzonatate
Generic Name benzonatate
Labeler camber pharmaceuticals, inc.
Dosage Form CAPSULE
Routes
ORAL
Active Ingredients

benzonatate 200 mg/1

Manufacturer
Camber Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 31722-958
Product ID 31722-958_30c74d00-0712-4c09-a7dc-6d1866860f03
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)
non-narcotic antitussive [epc]
Physiologic Effect
decreased tracheobronchial stretch receptor activity [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 31722958
Hyphenated Format 31722-958

Supplemental Identifiers

RxCUI
197397 283417 903291
UNII
5P4DHS6ENR
NUI
N0000009010 N0000175796

Packaging Origin

Original Packager
true

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
ORAL
source: ndc

Resolved Composition

Strengths
  • 200 mg/1
source: ndc
Packaging
  • 100 CAPSULE in 1 BOTTLE (31722-958-01)
  • 500 CAPSULE in 1 BOTTLE (31722-958-05)
  • 30 CAPSULE in 1 BOTTLE (31722-958-30)
source: ndc

Packages (3)

31722-958-01 100 CAPSULE in 1 BOTTLE (31722-958-01) 31722-958-05 500 CAPSULE in 1 BOTTLE (31722-958-05) 31722-958-30 30 CAPSULE in 1 BOTTLE (31722-958-30)

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": "30c74d00-0712-4c09-a7dc-6d1866860f03", "openfda": {"nui": ["N0000009010", "N0000175796"], "unii": ["5P4DHS6ENR"], "rxcui": ["197397", "283417", "903291"], "spl_set_id": ["c21afd18-3b04-4f15-874b-25e0c768f801"], "pharm_class_pe": ["Decreased Tracheobronchial Stretch Receptor Activity [PE]"], "pharm_class_epc": ["Non-narcotic Antitussive [EPC]"], "manufacturer_name": ["Camber Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (31722-958-01)", "package_ndc": "31722-958-01", "marketing_start_date": "20190222"}, {"sample": false, "description": "500 CAPSULE in 1 BOTTLE (31722-958-05)", "package_ndc": "31722-958-05", "marketing_start_date": "20190222"}, {"sample": false, "description": "30 CAPSULE in 1 BOTTLE (31722-958-30)", "package_ndc": "31722-958-30", "marketing_start_date": "20190222"}], "brand_name": "Benzonatate", "product_id": "31722-958_30c74d00-0712-4c09-a7dc-6d1866860f03", "dosage_form": "CAPSULE", "pharm_class": ["Decreased Tracheobronchial Stretch Receptor Activity [PE]", "Non-narcotic Antitussive [EPC]"], "product_ndc": "31722-958", "generic_name": "Benzonatate", "labeler_name": "Camber Pharmaceuticals, Inc.", "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"}