NDC 17478-312

Olopatadine

Olopatadine Hydrochloride

Olopatadine is a Ophthalmic Solution/ Drops in the Human Otc Drug category. It is labeled and distributed by Akorn. The primary component is Olopatadine Hydrochloride.

Product ID17478-312_4df9962a-31a1-454d-9e4a-a86927409e5e
NDC17478-312
Product TypeHuman Otc Drug
Proprietary NameOlopatadine
Generic NameOlopatadine Hydrochloride
Dosage FormSolution/ Drops
Route of AdministrationOPHTHALMIC
Marketing Start Date2021-09-01
Marketing CategoryANDA /
Application NumberANDA204723
Labeler NameAkorn
Substance NameOLOPATADINE HYDROCHLORIDE
Active Ingredient Strength2 mg/mL
Pharm ClassesDecreased Histamine Release [PE], Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC], Histamine-1 Receptor Inhibitor [EPC], Mast Cell Stabilizer [EPC]
NDC Exclude FlagN
Listing Certified Through2023-12-31

Packaging

NDC 17478-312-12

1 BOTTLE, DROPPER in 1 CARTON (17478-312-12) > 2.5 mL in 1 BOTTLE, DROPPER
Marketing Start Date2021-09-01
NDC Exclude FlagN
Sample Package?N

Drug Details

NDC Crossover Matching brand name "Olopatadine" or generic name "Olopatadine Hydrochloride"

NDCBrand NameGeneric Name
17478-105OlopatadineOlopatadine Hydrochloride
17478-305OlopatadineOlopatadine Hydrochloride
50090-3489OlopatadineOlopatadine
50090-3552OlopatadineOlopatadine
60429-957OlopatadineOlopatadine
0093-7684Olopatadine HydrochlorideOlopatadine Hydrochloride
0363-0200OLOPATADINE HYDROCHLORIDEOLOPATADINE HYDROCHLORIDE
0363-8022OLOPATADINE HYDROCHLORIDEOLOPATADINE HYDROCHLORIDE
0378-8023Olopatadine HydrochlorideOlopatadine Hydrochloride
0065-0272PATADAYolopatadine hydrochloride
0065-0816PATADAY ONCE DAILY RELIEFOLOPATADINE HYDROCHLORIDE
0065-8150PATADAY ONCE DAILY RELIEFOLOPATADINE HYDROCHLORIDE
0065-4274PATADAY TWICE A DAY RELIEFOLOPATADINE HYDROCHLORIDE
0065-0332PATANASEolopatadine hydrochloride
0078-0834PATANASEolopatadine hydrochloride
0065-0271Patanololopatadine hydrochloride
0065-4273Pazeoolopatadine hydrochloride

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