ALAVERT ALLERGY

Product NDC
0573-2620
11-digit product format
005732620
Labeler code
0573
Product ID
0573-2620_1ad9e626-55ca-4d43-b5ec-cc4d5bf19b07
Type
HUMAN OTC DRUG
Nonproprietary name
loratadine
Dosage form
TABLET, ORALLY DISINTEGRATING
Route
ORAL
Labeler
GlaxoSmithKline Consumer Healthcare Holdings (US) LLC
Application
NDA021375
Marketing category
NDA
Marketing start
2002-12-19
Marketing end
0000-00-00
Substance
LORATADINE
Active strength
10 mg/1
NDC exclude flag
No
Listing certified through
2021-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
0573-2620-06EA - Each0573-2620a426c267-75e5-4ee7-9ccb-d16f65916fb812013-02-11
0573-2620-19EA - Each0573-2620803dfd04-b25f-4194-9168-06ac1786360912012-07-24
0573-2620-30EA - Each0573-26207da8de28-0e7a-453a-81e4-006ec98783a212014-01-04
0573-2620-65EA - Each0573-2620526cf195-dcb5-4dc1-ab35-715787f1e3d712012-07-24

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
0573-2620-010057326200150 POUCH in 1 BOX (0573-2620-01) > 1 TABLET, ORALLY DISINTEGRATING in 1 POUCH50 pouch2002-12-190000-00-00NoNoCurrent
0573-2620-190057326201918 BLISTER PACK in 1 CARTON (0573-2620-19) > 1 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK18 blister pack2002-12-190000-00-00NoNoCurrent
0573-2620-650057326206560 BLISTER PACK in 1 CARTON (0573-2620-65) > 1 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK60 blister pack2002-12-190000-00-00NoNoCurrent
0573-2620-71005732620711500 POUCH in 1 BOX (0573-2620-71) > 1 TABLET, ORALLY DISINTEGRATING in 1 POUCH1500 pouch2002-12-190000-00-00NoNoCurrent