Loratadine

Product NDC
68071-2208
11-digit product format
680712208
Labeler code
68071
Product ID
68071-2208_de3404df-a314-d1e0-e053-2a95a90acbe8
Type
HUMAN OTC DRUG
Nonproprietary name
Loratadine
Dosage form
TABLET
Route
ORAL
Labeler
NuCare Pharmaceuticals,Inc.
Application
ANDA075209
Marketing category
ANDA
Marketing start
2019-12-27
Marketing end
0000-00-00
Substance
LORATADINE
Active strength
10 mg/1
NDC exclude flag
No
Listing certified through
2023-12-31
Current FDA listing
Historical FDA.report record

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
68071-2208LORATADINE NON DROWSY (LORATADINE) TABLET [NUCARE PHARMACEUTICALS,INC.]7Legacy NDC20240719_a9cb03e2-c508-1036-e053-2995a90a3683.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
68071-2208-3680712208031 BOTTLE, PLASTIC in 1 BOX (68071-2208-3) > 30 TABLET in 1 BOTTLE, PLASTIC2020-07-060000-00-00NoNoCurrent
68071-2208-4680712208041 BOTTLE, PLASTIC in 1 BOX (68071-2208-4) > 14 TABLET in 1 BOTTLE, PLASTIC2020-07-060000-00-00NoNoCurrent
68071-2208-6680712208061 BOTTLE, PLASTIC in 1 BOX (68071-2208-6) > 60 TABLET in 1 BOTTLE, PLASTIC2020-07-060000-00-00NoNoCurrent
68071-2208-7680712208071 BOTTLE, PLASTIC in 1 BOX (68071-2208-7) > 100 TABLET in 1 BOTTLE, PLASTIC2020-07-060000-00-00NoNoCurrent
68071-2208-9680712208091 BOTTLE, PLASTIC in 1 BOX (68071-2208-9) > 90 TABLET in 1 BOTTLE, PLASTIC2020-07-060000-00-00NoNoCurrent