Tessalon

Product NDC
0069-0122
11-digit product format
000690122
Labeler code
0069
Product ID
0069-0122_8dbb3489-c909-4df6-bd52-375d642f160e
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
benzonatate
Dosage form
CAPSULE
Route
ORAL
Labeler
Pfizer Laboratories Div Pfizer Inc
Application
NDA011210
Marketing category
NDA
Marketing start
1958-02-10
Marketing end
2022-05-31
Substance
BENZONATATE
Active strength
100 mg/1
Pharmacologic classes
Decreased Tracheobronchial Stretch Receptor Activity [PE],Non-narcotic Antitussive [EPC]
NDC exclude flag
No
Listing certified through
0000-00-00
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
0069-0122-01EA - Each0069-012267fddb04-2949-4c71-8df6-1d132229e9a312013-02-13

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
0069-0122-0100069012201100 CAPSULE in 1 BOTTLE (0069-0122-01) 100 capsule1958-02-100000-00-00NoNoCurrent