NDC 17478-308

Olopatadine

Olopatadine Hydrochloride

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

Product ID17478-308_3d190a3e-1484-4eac-8268-76399aefc4a2
NDC17478-308
Product TypeHuman Otc Drug
Proprietary NameOlopatadine
Generic NameOlopatadine Hydrochloride
Dosage FormSolution/ Drops
Route of AdministrationOPHTHALMIC
Marketing Start Date2021-09-01
Marketing CategoryANDA /
Application NumberANDA204532
Labeler NameAkorn, Inc.
Substance NameOLOPATADINE HYDROCHLORIDE
Active Ingredient Strength1 mg/mL
NDC Exclude FlagN
Listing Certified Through2022-12-31

Packaging

NDC 17478-308-05

1 BOTTLE, DROPPER in 1 CARTON (17478-308-05) > 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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