NDC 0440-7185

benzonatate

Benzonatate

benzonatate is a Oral Capsule in the Human Prescription Drug category. It is labeled and distributed by Liberty Pharmaceuticals, Inc.. The primary component is Benzonatate.

Product ID0440-7185_58e759cf-f686-453c-9575-91f74b00350a
NDC0440-7185
Product TypeHuman Prescription Drug
Proprietary Namebenzonatate
Generic NameBenzonatate
Dosage FormCapsule
Route of AdministrationORAL
Marketing Start Date2007-07-25
Marketing CategoryANDA / ANDA
Application NumberANDA040627
Labeler NameLiberty Pharmaceuticals, Inc.
Substance NameBENZONATATE
Active Ingredient Strength100 mg/1
Pharm ClassesDecreased Tracheobronchial Stretch Receptor Activity [PE],Non-narcotic Antitussive [EPC]
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 0440-7185-20

20 CAPSULE in 1 BOTTLE, PLASTIC (0440-7185-20)
Marketing Start Date2007-07-25
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 0440-7185-05 [00440718505]

benzonatate CAPSULE
Marketing CategoryANDA
Application NumberANDA040627
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2007-07-25
Marketing End Date2019-10-15

NDC 0440-7185-20 [00440718520]

benzonatate CAPSULE
Marketing CategoryANDA
Application NumberANDA040627
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2007-07-25
Marketing End Date2019-10-15

NDC 0440-7185-09 [00440718509]

benzonatate CAPSULE
Marketing CategoryANDA
Application NumberANDA040627
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2007-07-25
Marketing End Date2019-10-15

NDC 0440-7185-10 [00440718510]

benzonatate CAPSULE
Marketing CategoryANDA
Application NumberANDA040627
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2007-07-25
Marketing End Date2019-10-15

NDC 0440-7185-30 [00440718530]

benzonatate CAPSULE
Marketing CategoryANDA
Application NumberANDA040627
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2007-07-25
Marketing End Date2019-10-15

NDC 0440-7185-21 [00440718521]

benzonatate CAPSULE
Marketing CategoryANDA
Application NumberANDA040627
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2007-07-25
Marketing End Date2019-10-15

NDC 0440-7185-01 [00440718501]

benzonatate CAPSULE
Marketing CategoryANDA
Application NumberANDA040627
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2007-07-25
Marketing End Date2019-10-15

NDC 0440-7185-81 [00440718581]

benzonatate CAPSULE
Marketing CategoryANDA
Application NumberANDA040627
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2007-07-25
Marketing End Date2019-10-15

NDC 0440-7185-15 [00440718515]

benzonatate CAPSULE
Marketing CategoryANDA
Application NumberANDA040627
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2007-07-25
Marketing End Date2019-10-15

Drug Details

Active Ingredients

IngredientStrength
BENZONATATE100 mg/1

OpenFDA Data

SPL SET ID:820521d1-ea64-4a06-bcf9-e2d7700d371c
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 197397
  • 283417
  • Pharmacological Class

    • Decreased Tracheobronchial Stretch Receptor Activity [PE]
    • Non-narcotic Antitussive [EPC]

    NDC Crossover Matching brand name "benzonatate" or generic name "Benzonatate"

    NDCBrand NameGeneric Name
    0179-0237benzonatatebenzonatate
    0440-1185benzonatatebenzonatate
    0440-5185benzonatatebenzonatate
    0440-5186benzonatatebenzonatate
    0440-5187benzonatatebenzonatate
    0440-7185benzonatatebenzonatate
    0440-7186benzonatatebenzonatate
    0615-1349BenzonatateBenzonatate
    0615-7678BenzonatateBenzonatate
    0615-7887benzonatatebenzonatate
    0615-8143benzonatatebenzonatate
    0615-8194benzonatatebenzonatate
    0615-8403BenzonatateBenzonatate
    0904-5904benzonatatebenzonatate
    0904-5905benzonatatebenzonatate
    0904-6564BenzonatateBenzonatate
    0904-6657benzonatatebenzonatate
    0904-7153BenzonatateBenzonatate
    10135-632BenzonatateBenzonatate
    10544-094benzonatatebenzonatate
    10544-123benzonatatebenzonatate
    10544-129benzonatatebenzonatate
    11788-027benzonatatebenzonatate
    11788-028benzonatatebenzonatate
    11788-029benzonatatebenzonatate
    67877-128benzonatatebenzonatate
    67877-105benzonatatebenzonatate
    67877-106benzonatatebenzonatate
    67877-575benzonatatebenzonatate
    67877-574benzonatatebenzonatate
    67877-573benzonatatebenzonatate
    68071-1891benzonatatebenzonatate
    68071-1984benzonatatebenzonatate
    68071-3185benzonatatebenzonatate
    68071-1877BenzonatateBenzonatate
    68071-3204benzonatatebenzonatate
    68071-3346benzonatatebenzonatate
    68071-4317benzonatatebenzonatate
    68071-4105BenzonatateBenzonatate
    68071-4258benzonatatebenzonatate
    68071-4337benzonatatebenzonatate
    68071-4276benzonatatebenzonatate
    68151-2697BenzonatateBenzonatate
    68382-247BenzonatateBenzonatate
    68382-248BenzonatateBenzonatate
    68788-6357BenzonatateBenzonatate
    68788-7014BenzonatateBenzonatate
    68788-6839BenzonatateBenzonatate
    68788-7087benzonatatebenzonatate
    68788-7094benzonatatebenzonatate

    © 2024 FDA.report
    This site is not affiliated with or endorsed by the FDA.