Benzonatate

Product NDC
68382-248
11-digit product format
683820248
Labeler code
68382
Product ID
68382-248_c3051916-c62a-441f-84ce-5b2fd415af03
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Benzonatate
Dosage form
CAPSULE
Route
ORAL
Labeler
Zydus Pharmaceuticals (USA) Inc.
Application
ANDA040597
Marketing category
ANDA
Marketing start
2007-04-09
Marketing end
0000-00-00
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
2021-12-31
Current FDA listing
Historical FDA.report record

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
dc429dc2-e942-6686-8d72-b63c57e806aaProduct name520190416
d45c2ed6-126c-dd22-afd2-e29a2ecf77b9Product name320190215

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
68382-248-01EA - Each68382-2488de897ab-ba1c-41e8-9a2e-89151fbd4b9012012-07-24

DailyMed Socrata Ingredients#

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
197397benzonatate 100 MG Oral CapsulePSNe0f1b5cf-863c-42fa-acd9-43a7e30b40542
283417benzonatate 200 MG Oral CapsulePSNe0f1b5cf-863c-42fa-acd9-43a7e30b40542
197397benzonatate 100 MG Oral CapsuleSCDe0f1b5cf-863c-42fa-acd9-43a7e30b40542
283417benzonatate 200 MG Oral CapsuleSCDe0f1b5cf-863c-42fa-acd9-43a7e30b40542

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
68382-248-0168382024801100 CAPSULE in 1 BOTTLE (68382-248-01) 100 capsule2007-04-090000-00-00NoNoCurrent