PATADAY

Product NDC
0065-0272
11-digit product format
000650272
Labeler code
0065
Product ID
0065-0272_593964bd-f972-427b-8b11-802c94ca2b11
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
olopatadine hydrochloride
Dosage form
SOLUTION/ DROPS
Route
OPHTHALMIC
Labeler
Alcon Laboratories, Inc.
Application
NDA021545
Marketing category
NDA
Marketing start
2007-02-15
Marketing end
2021-09-30
Substance
OLOPATADINE HYDROCHLORIDE
Active strength
2 mg/mL
Pharmacologic classes
Decreased Histamine Release [PE],Histamine H1 Receptor Antagonists [MoA],Histamine-1 Receptor Inhibitor [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
0065-0272-25ML - Milliliter0065-0272cad510e4-8a94-4704-8c78-69e9daf66a0e12012-07-24

DailyMed Socrata Ingredients#

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
0065-0272-11000650272111 POUCH in 1 CARTON (0065-0272-11) > 1 BOTTLE in 1 POUCH > .5 mL in 1 BOTTLE1 pouch2007-02-152021-09-30NoNoCurrent
0065-0272-25000650272251 BOTTLE, PLASTIC in 1 CARTON (0065-0272-25) > 2.5 mL in 1 BOTTLE, PLASTIC2007-02-152021-09-30NoNoCurrent