NDC 0456-2010-11 - Lexapro

This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.

Product NDC: 0456-2010
Requested NDC: 0456-2010-11
Package NDCs from labels: 0456-2010-01, 0456-2010-11, 0456-2010-63
Manufacturer: Allergan, Inc.
Effective date: 2023-10-01
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
Lexapro - Allergan, Inc.	Allergan, Inc.	2023-10-01	HUMAN PRESCRIPTION DRUG LABEL
Lexapro - PD-Rx Pharmaceuticals, Inc.	PD-Rx Pharmaceuticals, Inc.	2022-03-21	HUMAN PRESCRIPTION DRUG LABEL
Lexapro - Aidarex Pharmaceuticals LLC	Aidarex Pharmaceuticals LLC	2014-01-08	HUMAN PRESCRIPTION DRUG LABEL
LEXAPRO - STAT Rx USA LLC \| PSS WORLD MEDICAL INC	STAT Rx USA LLC \| PSS WORLD MEDICAL INC	2012-07-16	HUMAN PRESCRIPTION DRUG LABEL
Lexapro - Physicians Total Care, Inc.	Physicians Total Care, Inc.	2010-01-12	HUMAN PRESCRIPTION DRUG LABEL
National Council for Prescription Drug Programs indexing - billing unit	National Council for Prescription Drug Programs	2013-02-13	Indexing - Billing Unit

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
0456-2010-01	Lexapro	100 in 1 BOTTLE	TABLET, FILM COATED	100	45
0456-2010-11	Lexapro	10 in 1 BLISTER PACK	TABLET, FILM COATED	10	45
0456-2010-63	Lexapro	10 in 1 BOX, UNIT-DOSE	TABLET, FILM COATED	10	45

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
0456-2010	LEXAPRO (ESCITALOPRAM) TABLET, FILM COATED LEXAPRO (ESCITALOPRAM) SOLUTION [ALLERGAN, INC.]	44	Current NDC, Legacy NDC, 3 package rows	20240501_13bb8267-1cab-43e5-acae-55a4d957630a.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
0456-2010-01	EA - Each	0456-2010	fb8e1267-e81a-4a0e-a34a-1181e245dba2	1	2012-07-24
0456-2010-11	EA - Each	0456-2010	2517c551-4fd2-495c-b134-fd1e8725be60	1	2013-02-13
0456-2010-63	EA - Each	0456-2010	07d15662-4d29-49d7-8069-2720ba51d13b	1	2012-07-24

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
ESCITALOPRAM OXALATE	ACTIVE INGREDIENT	5U85DBW7LO	LEXAPRO (ESCITALOPRAM OXALATE) TABLET, FILM COATED LEXAPRO (ESCITALOPRAM OXALATE) SOLUTION [FOREST LABORATORIES, INC.]	18
ESCITALOPRAM	ACTIVE MOIETY	4O4S742ANY	LEXAPRO (ESCITALOPRAM OXALATE) TABLET, FILM COATED LEXAPRO (ESCITALOPRAM OXALATE) SOLUTION [FOREST LABORATORIES, INC.]	18
CELLULOSE, MICROCRYSTALLINE	INACTIVE INGREDIENT	OP1R32D61U	LEXAPRO (ESCITALOPRAM OXALATE) TABLET, FILM COATED LEXAPRO (ESCITALOPRAM OXALATE) SOLUTION [FOREST LABORATORIES, INC.]	18
CITRIC ACID MONOHYDRATE	INACTIVE INGREDIENT	2968PHW8QP	LEXAPRO (ESCITALOPRAM OXALATE) TABLET, FILM COATED LEXAPRO (ESCITALOPRAM OXALATE) SOLUTION [FOREST LABORATORIES, INC.]	18
CROSCARMELLOSE SODIUM	INACTIVE INGREDIENT	M28OL1HH48	LEXAPRO (ESCITALOPRAM OXALATE) TABLET, FILM COATED LEXAPRO (ESCITALOPRAM OXALATE) SOLUTION [FOREST LABORATORIES, INC.]	18
GLYCERIN	INACTIVE INGREDIENT	PDC6A3C0OX	LEXAPRO (ESCITALOPRAM OXALATE) TABLET, FILM COATED LEXAPRO (ESCITALOPRAM OXALATE) SOLUTION [FOREST LABORATORIES, INC.]	18
HYPROMELLOSES	INACTIVE INGREDIENT	3NXW29V3WO	LEXAPRO (ESCITALOPRAM OXALATE) TABLET, FILM COATED LEXAPRO (ESCITALOPRAM OXALATE) SOLUTION [FOREST LABORATORIES, INC.]	18
MAGNESIUM STEARATE	INACTIVE INGREDIENT	70097M6I30	LEXAPRO (ESCITALOPRAM OXALATE) TABLET, FILM COATED LEXAPRO (ESCITALOPRAM OXALATE) SOLUTION [FOREST LABORATORIES, INC.]	18
MALIC ACID	INACTIVE INGREDIENT	817L1N4CKP	LEXAPRO (ESCITALOPRAM OXALATE) TABLET, FILM COATED LEXAPRO (ESCITALOPRAM OXALATE) SOLUTION [FOREST LABORATORIES, INC.]	18
METHYLPARABEN	INACTIVE INGREDIENT	A2I8C7HI9T	LEXAPRO (ESCITALOPRAM OXALATE) TABLET, FILM COATED LEXAPRO (ESCITALOPRAM OXALATE) SOLUTION [FOREST LABORATORIES, INC.]	18
PEPPERMINT	INACTIVE INGREDIENT	V95R5KMY2B	LEXAPRO (ESCITALOPRAM OXALATE) TABLET, FILM COATED LEXAPRO (ESCITALOPRAM OXALATE) SOLUTION [FOREST LABORATORIES, INC.]	18
POLYETHYLENE GLYCOLS	INACTIVE INGREDIENT	3WJQ0SDW1A	LEXAPRO (ESCITALOPRAM OXALATE) TABLET, FILM COATED LEXAPRO (ESCITALOPRAM OXALATE) SOLUTION [FOREST LABORATORIES, INC.]	18
PROPYLENE GLYCOL	INACTIVE INGREDIENT	6DC9Q167V3	LEXAPRO (ESCITALOPRAM OXALATE) TABLET, FILM COATED LEXAPRO (ESCITALOPRAM OXALATE) SOLUTION [FOREST LABORATORIES, INC.]	18
PROPYLPARABEN	INACTIVE INGREDIENT	Z8IX2SC1OH	LEXAPRO (ESCITALOPRAM OXALATE) TABLET, FILM COATED LEXAPRO (ESCITALOPRAM OXALATE) SOLUTION [FOREST LABORATORIES, INC.]	18
SILICON DIOXIDE	INACTIVE INGREDIENT	ETJ7Z6XBU4	LEXAPRO (ESCITALOPRAM OXALATE) TABLET, FILM COATED LEXAPRO (ESCITALOPRAM OXALATE) SOLUTION [FOREST LABORATORIES, INC.]	18
SODIUM CITRATE	INACTIVE INGREDIENT	1Q73Q2JULR	LEXAPRO (ESCITALOPRAM OXALATE) TABLET, FILM COATED LEXAPRO (ESCITALOPRAM OXALATE) SOLUTION [FOREST LABORATORIES, INC.]	18
SORBITOL	INACTIVE INGREDIENT	506T60A25R	LEXAPRO (ESCITALOPRAM OXALATE) TABLET, FILM COATED LEXAPRO (ESCITALOPRAM OXALATE) SOLUTION [FOREST LABORATORIES, INC.]	18
TALC	INACTIVE INGREDIENT	7SEV7J4R1U	LEXAPRO (ESCITALOPRAM OXALATE) TABLET, FILM COATED LEXAPRO (ESCITALOPRAM OXALATE) SOLUTION [FOREST LABORATORIES, INC.]	18
TITANIUM DIOXIDE	INACTIVE INGREDIENT	15FIX9V2JP	LEXAPRO (ESCITALOPRAM OXALATE) TABLET, FILM COATED LEXAPRO (ESCITALOPRAM OXALATE) SOLUTION [FOREST LABORATORIES, INC.]	18
WATER	INACTIVE INGREDIENT	059QF0KO0R	LEXAPRO (ESCITALOPRAM OXALATE) TABLET, FILM COATED LEXAPRO (ESCITALOPRAM OXALATE) SOLUTION [FOREST LABORATORIES, INC.]	18
ESCITALOPRAM OXALATE	ACTIVE INGREDIENT	5U85DBW7LO	LEXAPRO (ESCITALOPRAM OXALATE) TABLET, FILM COATED [PD-RX PHARMACEUTICALS, INC.]	14
ESCITALOPRAM	ACTIVE MOIETY	4O4S742ANY	LEXAPRO (ESCITALOPRAM OXALATE) TABLET, FILM COATED [PD-RX PHARMACEUTICALS, INC.]	14
CELLULOSE, MICROCRYSTALLINE	INACTIVE INGREDIENT	OP1R32D61U	LEXAPRO (ESCITALOPRAM OXALATE) TABLET, FILM COATED [PD-RX PHARMACEUTICALS, INC.]	14
CROSCARMELLOSE SODIUM	INACTIVE INGREDIENT	M28OL1HH48	LEXAPRO (ESCITALOPRAM OXALATE) TABLET, FILM COATED [PD-RX PHARMACEUTICALS, INC.]	14
HYPROMELLOSES	INACTIVE INGREDIENT	3NXW29V3WO	LEXAPRO (ESCITALOPRAM OXALATE) TABLET, FILM COATED [PD-RX PHARMACEUTICALS, INC.]	14
MAGNESIUM STEARATE	INACTIVE INGREDIENT	70097M6I30	LEXAPRO (ESCITALOPRAM OXALATE) TABLET, FILM COATED [PD-RX PHARMACEUTICALS, INC.]	14
POLYETHYLENE GLYCOL	INACTIVE INGREDIENT	3WJQ0SDW1A	LEXAPRO (ESCITALOPRAM OXALATE) TABLET, FILM COATED [PD-RX PHARMACEUTICALS, INC.]	14
SILICON DIOXIDE	INACTIVE INGREDIENT	ETJ7Z6XBU4	LEXAPRO (ESCITALOPRAM OXALATE) TABLET, FILM COATED [PD-RX PHARMACEUTICALS, INC.]	14
TALC	INACTIVE INGREDIENT	7SEV7J4R1U	LEXAPRO (ESCITALOPRAM OXALATE) TABLET, FILM COATED [PD-RX PHARMACEUTICALS, INC.]	14
TITANIUM DIOXIDE	INACTIVE INGREDIENT	15FIX9V2JP	LEXAPRO (ESCITALOPRAM OXALATE) TABLET, FILM COATED [PD-RX PHARMACEUTICALS, INC.]	14
ESCITALOPRAM OXALATE	ACTIVE INGREDIENT	5U85DBW7LO	LEXAPRO (ESCITALOPRAM OXALATE) TABLET, FILM COATED [STAT RX USA LLC]	2
ESCITALOPRAM	ACTIVE MOIETY	4O4S742ANY	LEXAPRO (ESCITALOPRAM OXALATE) TABLET, FILM COATED [STAT RX USA LLC]	2
CELLULOSE, MICROCRYSTALLINE	INACTIVE INGREDIENT	OP1R32D61U	LEXAPRO (ESCITALOPRAM OXALATE) TABLET, FILM COATED [STAT RX USA LLC]	2
CROSCARMELLOSE SODIUM	INACTIVE INGREDIENT	M28OL1HH48	LEXAPRO (ESCITALOPRAM OXALATE) TABLET, FILM COATED [STAT RX USA LLC]	2
HYPROMELLOSES	INACTIVE INGREDIENT	3NXW29V3WO	LEXAPRO (ESCITALOPRAM OXALATE) TABLET, FILM COATED [STAT RX USA LLC]	2
MAGNESIUM STEARATE	INACTIVE INGREDIENT	70097M6I30	LEXAPRO (ESCITALOPRAM OXALATE) TABLET, FILM COATED [STAT RX USA LLC]	2
POLYETHYLENE GLYCOLS	INACTIVE INGREDIENT	3WJQ0SDW1A	LEXAPRO (ESCITALOPRAM OXALATE) TABLET, FILM COATED [STAT RX USA LLC]	2
SILICON DIOXIDE	INACTIVE INGREDIENT	ETJ7Z6XBU4	LEXAPRO (ESCITALOPRAM OXALATE) TABLET, FILM COATED [STAT RX USA LLC]	2
TALC	INACTIVE INGREDIENT	7SEV7J4R1U	LEXAPRO (ESCITALOPRAM OXALATE) TABLET, FILM COATED [STAT RX USA LLC]	2
TITANIUM DIOXIDE	INACTIVE INGREDIENT	15FIX9V2JP	LEXAPRO (ESCITALOPRAM OXALATE) TABLET, FILM COATED [STAT RX USA LLC]	2
ESCITALOPRAM OXALATE	ACTIVE INGREDIENT	5U85DBW7LO	LEXAPRO (ESCITALOPRAM OXALATE) TABLET, FILM COATED [AIDAREX PHARMACEUTICALS LLC]	1
ESCITALOPRAM OXALATE	ACTIVE INGREDIENT	5U85DBW7LO	LEXAPRO (ESCITALOPRAM OXALATE) TABLET [PHYSICIANS TOTAL CARE, INC.]	1
ESCITALOPRAM	ACTIVE MOIETY	4O4S742ANY	LEXAPRO (ESCITALOPRAM OXALATE) TABLET, FILM COATED [AIDAREX PHARMACEUTICALS LLC]	1
ESCITALOPRAM	ACTIVE MOIETY	4O4S742ANY	LEXAPRO (ESCITALOPRAM OXALATE) TABLET [PHYSICIANS TOTAL CARE, INC.]	1
CELLULOSE, MICROCRYSTALLINE	INACTIVE INGREDIENT	OP1R32D61U	LEXAPRO (ESCITALOPRAM OXALATE) TABLET, FILM COATED [AIDAREX PHARMACEUTICALS LLC]	1
CROSCARMELLOSE SODIUM	INACTIVE INGREDIENT	M28OL1HH48	LEXAPRO (ESCITALOPRAM OXALATE) TABLET, FILM COATED [AIDAREX PHARMACEUTICALS LLC]	1
CROSCARMELLOSE SODIUM	INACTIVE INGREDIENT	M28OL1HH48	LEXAPRO (ESCITALOPRAM OXALATE) TABLET [PHYSICIANS TOTAL CARE, INC.]	1
HYPROMELLOSES	INACTIVE INGREDIENT	3NXW29V3WO	LEXAPRO (ESCITALOPRAM OXALATE) TABLET, FILM COATED [AIDAREX PHARMACEUTICALS LLC]	1
MAGNESIUM STEARATE	INACTIVE INGREDIENT	70097M6I30	LEXAPRO (ESCITALOPRAM OXALATE) TABLET, FILM COATED [AIDAREX PHARMACEUTICALS LLC]	1
MAGNESIUM STEARATE	INACTIVE INGREDIENT	70097M6I30	LEXAPRO (ESCITALOPRAM OXALATE) TABLET [PHYSICIANS TOTAL CARE, INC.]	1
POLYETHYLENE GLYCOLS	INACTIVE INGREDIENT	3WJQ0SDW1A	LEXAPRO (ESCITALOPRAM OXALATE) TABLET, FILM COATED [AIDAREX PHARMACEUTICALS LLC]	1
SILICON DIOXIDE	INACTIVE INGREDIENT	ETJ7Z6XBU4	LEXAPRO (ESCITALOPRAM OXALATE) TABLET [PHYSICIANS TOTAL CARE, INC.]	1
SILICON DIOXIDE	INACTIVE INGREDIENT	ETJ7Z6XBU4	LEXAPRO (ESCITALOPRAM OXALATE) TABLET, FILM COATED [AIDAREX PHARMACEUTICALS LLC]	1
TALC	INACTIVE INGREDIENT	7SEV7J4R1U	LEXAPRO (ESCITALOPRAM OXALATE) TABLET [PHYSICIANS TOTAL CARE, INC.]	1
TALC	INACTIVE INGREDIENT	7SEV7J4R1U	LEXAPRO (ESCITALOPRAM OXALATE) TABLET, FILM COATED [AIDAREX PHARMACEUTICALS LLC]	1
TITANIUM DIOXIDE	INACTIVE INGREDIENT	15FIX9V2JP	LEXAPRO (ESCITALOPRAM OXALATE) TABLET, FILM COATED [AIDAREX PHARMACEUTICALS LLC]	1

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 2 of 168 · 3,356 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Aging Eye Formula	CINERARIA MARITIMA, EYE (SUIS), CALCAREA FLUORICA, CAUSTICUM, PHOSPHORUS, SILICEA, ZINCUM METALLICUM, GERMANIUM METALLICUM, NATRUM MURIATICUM	Nutritional Specialties, Inc.	d5b44f79-5299-4b31-ba45-0e511cdbe17c	2026-08-24	Warnings	Exact identifier unii: ETJ7Z6XBU4
Rohto Optic Glow	NAPHAZOLINE HYDROCHLORIDE, POVIDONE, PROPYLENE GLYCOL	The Mentholatum Company	df9c5f7c-96e6-4b2b-b8cb-21a6a3342dff	2026-08-20	Warnings	Exact identifier unii: 6DC9Q167V3
Rohto All-In-One	HYPROMELLOSE, TETRAHYDROZOLINE HYDROCHLORIDE, ZINC SULFATE	The Mentholatum Company	43e690e4-b381-46e3-838c-33aef5bdadde	2026-08-20	Warnings	Exact identifier unii: 3NXW29V3WO
Bio Combination 28	SCHUESSLER SALTS	LDD Bioscience Private Limited	597caf33-5107-9dec-e063-6294a90a5fcd	2026-08-20	Warnings	Exact identifier unii: ETJ7Z6XBU4
Sweat Resistant Sunscreen Body Original	TITANIUM DIOXIDE, ZINC OXIDE	Clutch, Inc.	4bbde755-e312-123e-e063-6294a90a467f	2026-08-20	Warnings	Exact identifier unii: 15FIX9V2JP
Psorinum Complex	PHOSPHORUS, SILICEA, SULPHUR, ALOE	BioActive Nutritional, Inc.	d4746927-e6d4-463d-a084-56ffc48d1e67	2026-08-20	Warnings	Exact identifier unii: ETJ7Z6XBU4
Boneforce HP	CALCAREA CARBONICA, CALCAREA FLUORICA, CALCAREA PHOSPHORICA, HEKLA LAVA, HYDROFLUORICUM ACIDUM, RHUS TOX, SILICEA, SYMPHYTUM OFFICINALE	BioActive Nutritional, Inc.	d96ca52b-781d-431c-ad2a-a54fd57eb106	2026-08-20	Warnings	Exact identifier unii: ETJ7Z6XBU4
Rohto Preservative Free Dry Aid	POVIDONE, PROPYLENE GLYCOL	The Mentholatum Company	f4b1974c-2412-45f6-b79d-88b8a0bcb608	2026-08-18	Warnings	Exact identifier unii: 6DC9Q167V3
Rohto Dry-Aid	POVIDONE, PROPYLENE GLYCOL	The Mentholatum Company	8ea5c6c9-48f4-406a-a2cb-9280c546d87d	2026-08-18	Warnings	Exact identifier unii: 6DC9Q167V3
HEADHUNTER SURF SCREEN SPF 50 SUNSCREEN	ZINC OXIDE,TITANIUM DIOXIDE	Guangzhou Tata Biotechnology Co., Ltd.	4339df13-77d3-31a1-e063-6394a90a5208	2026-08-17	Warnings	Exact identifier unii: 15FIX9V2JP
Cerebellum Thalamus A Aurm	CEREBELLUM THALAMUS A AURUM	Uriel Pharmacy Inc.	e1c395b8-9221-401f-8980-c91ff8843458	2026-08-17	Warnings	Exact identifier unii: ETJ7Z6XBU4
Stay Ageless Tinted Mineral Sunscreen	BROAD SPECTRUM SPF30	HAMBLIN DERMATOLOGY	5942e64c-416e-7525-e063-6394a90a2839	2026-08-17	Warnings	Exact identifier unii: 15FIX9V2JP
Protect Tinted Mineral Sunscreen	BROAD SPECTRUM SPF30	Opal Day Spa	5943413a-48e1-0bdf-e063-6294a90a2fff	2026-08-17	Warnings	Exact identifier unii: 15FIX9V2JP
Stay Ageless Tinted Mineral Sunscreen	BROAD SPECTRUM SPF30	MedSpa By Beauty Bar LLC	5943ba3d-688e-9e9c-e063-6294a90afa9a	2026-08-17	Warnings	Exact identifier unii: 15FIX9V2JP
Stay Ageless Tinted Mineral Sunscreen	BROAD SPECTRUM SPF30	CORBY, JR., TERRY L.	594443fd-8e27-4ec6-e063-6294a90a3ff0	2026-08-17	Warnings	Exact identifier unii: 15FIX9V2JP
Leader Dry Eye Relief Eye Drops	GLYCERIN, HYPROMELLOSE, POLYETHYLENE GLYCOL 400	CARDINAL HEALTH 110, LLC. DBA LEADER	2ded4bda-b3c3-4521-8701-5c8446fd148b	2026-08-17	Warnings	Exact identifier unii: PDC6A3C0OX unii: 3NXW29V3WO
BM BM63 DROPS	CEANOTHUS, KALI ARSEN, KALI MUR, SELENIUM, THALLIUM, WIESBADEN	BM Private Limited	59006d82-610a-2e08-e063-6394a90af1ed	2026-08-14	Warnings	Exact identifier unii: 059QF0KO0R
BM BM134 DROPS	ARSENIC ALBUM, HYDRASTIS, MYRISTICA, NITRIC ACID, PAEONIA, RHUS TOX, SILICEA	BM Private Limited	59023500-89be-cc76-e063-6294a90a6e02	2026-08-14	Warnings	Exact identifier unii: ETJ7Z6XBU4
BM BM164 DROPS	ARUM TRYPH, CAUSTICUM, BALSAMUM PERU, HELONIAS DIO, ACID PHOS, GLYCERINUM, EQUISETUM	BM Private Limited	5902770f-eb01-d099-e063-6394a90ad3eb	2026-08-14	Warnings	Exact identifier unii: PDC6A3C0OX
BM BM173 DROPS	ECHINACEA, EUPHRASIA, NATRUM MUR, RHUS TOX, SILICEA, SULPHUR, URTICA UREN	BM Private Limited	59036ca4-e7bb-bbe7-e063-6394a90a410a	2026-08-14	Warnings	Exact identifier unii: ETJ7Z6XBU4

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.