Home NDC 82442-027-50 Eye Allergy Itch Relief
Product NDC 82442-027
Requested package NDC 82442-027-50
11-digit product format 824420027
Labeler code 82442
Product ID 82442-027_fc28766c-0cc5-996f-4332-7913d9b1c62d
Type HUMAN OTC DRUG
Nonproprietary name olopatadine hydrochloride
Dosage form SOLUTION/ DROPS
Route OPHTHALMIC
Labeler TARGET CORPORATION
Application ANDA213514
Marketing category ANDA
Marketing start 2026-08-15
Substance OLOPATADINE HYDROCHLORIDE
Active strength 7 mg/mL
Pharmacologic classes Decreased Histamine Release [PE], Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC], Histamine-1 Receptor Inhibitor [EPC], Mast Cell Stabilizer [EPC]
NDC exclude flag No
Listing certified through 2027-12-31
Current FDA listing Yes Source provenance: Browse the complete Orange Book source catalog · source snapshot 43 .
Orange Book products# Current product rows page 1 of 1 · 1 matching rows.
Application-product, Trade name, Ingredient table Application-product Trade name Ingredient Strength Dosage form / route TE codes RLD / RS Approval date A213514-001 OLOPATADINE HYDROCHLORIDE OLOPATADINE HYDROCHLORIDE EQ 0.7% BASE SOLUTION/DROPS / OPHTHALMIC 2026-01-06
Observed Orange Book product history# Observed FDA ZIP history: Each table is queried independently by exact application/product key from successfully parsed Orange Book snapshots. Capture times identify archived source observations; absence or a change between snapshots is not inferred. FDA publication files that were not recoverable as structured ZIP data are not represented as states.
Captured, Edition, Application-product table Captured Edition Application-product Trade name Strength Dosage form / route Product TE source text RLD / RS Approval date Source SHA-256 2026-09-14 22:38:34 2026-08 A213514-001 OLOPATADINE HYDROCHLORIDE EQ 0.7% BASE SOLUTION/DROPS / OPHTHALMIC 2026-01-06 84e616aacf4f…2026-08-18 06:07:40 2026-07 A213514-001 OLOPATADINE HYDROCHLORIDE EQ 0.7% BASE SOLUTION/DROPS / OPHTHALMIC 2026-01-06 caaa826d4ba7…2026-02-19 14:30 UTC 2026-02 A213514-001 OLOPATADINE HYDROCHLORIDE EQ 0.7% BASE SOLUTION/DROPS / OPHTHALMIC 2026-01-06 011fe1cb6892…2026-07-26 02:55 UTC · 3 captures of this ZIP 2026-06 A213514-001 OLOPATADINE HYDROCHLORIDE EQ 0.7% BASE SOLUTION/DROPS / OPHTHALMIC 2026-01-06 a50c72e98297…
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base Eye Allergy Itch Relief
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength OLOPATADINE HYDROCHLORIDE 7 mg/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 2XG66W44KF Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 1601086 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 1 of 1 · 9 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Marketing start Sample Exclude flag Status 82442-027-50 82442002750 2 BOTTLE, DROPPER in 1 CARTON (82442-027-50) / 2.5 mL in 1 BOTTLE, DROPPER 2026-08-15 No No Current