NDC 68788-7607

Benzonatate

Benzonatate

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

Product ID68788-7607_3309040d-e240-42f6-9c51-5c54604a3896
NDC68788-7607
Product TypeHuman Prescription Drug
Proprietary NameBenzonatate
Generic NameBenzonatate
Dosage FormCapsule
Route of AdministrationORAL
Marketing Start Date2020-02-07
Marketing CategoryANDA / ANDA
Application NumberANDA206948
Labeler NamePreferred 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 Through2021-12-31

Packaging

NDC 68788-7607-0

9 CAPSULE in 1 BOTTLE (68788-7607-0)
Marketing Start Date2020-02-07
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 68788-7607-3 [68788760703]

Benzonatate CAPSULE
Marketing CategoryANDA
Application NumberANDA206948
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2020-02-07

NDC 68788-7607-1 [68788760701]

Benzonatate CAPSULE
Marketing CategoryANDA
Application NumberANDA206948
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2020-02-07

NDC 68788-7607-0 [68788760700]

Benzonatate CAPSULE
Marketing CategoryANDA
Application NumberANDA206948
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2020-02-07

NDC 68788-7607-2 [68788760702]

Benzonatate CAPSULE
Marketing CategoryANDA
Application NumberANDA206948
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2020-02-07

NDC 68788-7607-5 [68788760705]

Benzonatate CAPSULE
Marketing CategoryANDA
Application NumberANDA206948
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2020-02-07

NDC 68788-7607-4 [68788760704]

Benzonatate CAPSULE
Marketing CategoryANDA
Application NumberANDA206948
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2020-02-07

NDC 68788-7607-9 [68788760709]

Benzonatate CAPSULE
Marketing CategoryANDA
Application NumberANDA206948
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2020-02-07

Drug Details

Active Ingredients

IngredientStrength
BENZONATATE100 mg/1

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

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