BENZONATATE

Product NDC
71335-2021
11-digit product format
713352021
Labeler code
71335
Product ID
71335-2021_e1c77f1a-79d0-4c5d-a011-fd5c8cd59ffe
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
BENZONATATE
Dosage form
CAPSULE
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
ANDA040682
Marketing category
ANDA
Marketing start
2018-05-01
Substance
BENZONATATE
Active strength
200 mg/1
Pharmacologic classes
Decreased Tracheobronchial Stretch Receptor Activity [PE], Non-narcotic Antitussive [EPC]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
BENZONATATE
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
BENZONATATE200 mg/1

Harmonized Identifiers#

Field, Values table
FieldValues
Unii5P4DHS6ENR
Rxcui283417

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
71335-2021-17133520210130 CAPSULE in 1 BOTTLE (71335-2021-1) 30 capsule2022-02-100000-00-00NoNoCurrent
71335-2021-271335202102100 CAPSULE in 1 BOTTLE (71335-2021-2) 100 capsule2022-02-100000-00-00NoNoCurrent
71335-2021-37133520210345 CAPSULE in 1 BOTTLE (71335-2021-3) 45 capsule2022-02-100000-00-00NoNoCurrent
71335-2021-47133520210420 CAPSULE in 1 BOTTLE (71335-2021-4) 20 capsule2022-02-100000-00-00NoNoCurrent
71335-2021-57133520210515 CAPSULE in 1 BOTTLE (71335-2021-5) 15 capsule2022-02-100000-00-00NoNoCurrent
71335-2021-67133520210621 CAPSULE in 1 BOTTLE (71335-2021-6) 21 capsule2022-02-100000-00-00NoNoCurrent
71335-2021-77133520210760 CAPSULE in 1 BOTTLE (71335-2021-7) 60 capsule2022-02-100000-00-00NoNoCurrent
71335-2021-87133520210850 CAPSULE in 1 BOTTLE (71335-2021-8) 50 capsule2022-02-100000-00-00NoNoCurrent
71335-2021-97133520210990 CAPSULE in 1 BOTTLE (71335-2021-9) 90 capsule2022-02-100000-00-00NoNoCurrent