NDC 43598-166-79 - Olanzapine

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: 43598-166
Requested NDC: 43598-166-79
Package NDCs from labels: 43598-166-30, 43598-166-60, 43598-166-01, 43598-166-05, 43598-166-10, 43598-166-79, 43598-166-78
Manufacturer: REMEDYREPACK INC.
Effective date: 2026-09-21
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
Olanzapine - REMEDYREPACK INC.	REMEDYREPACK INC.	2026-09-21	HUMAN PRESCRIPTION DRUG LABEL
Olanzapine - Major Pharmaceuticals	Major Pharmaceuticals	2026-07-08	HUMAN PRESCRIPTION DRUG LABEL
Olanzapine - REMEDYREPACK INC.	REMEDYREPACK INC.	2026-07-08	HUMAN PRESCRIPTION DRUG LABEL
Olanzapine - Unit Dose Solutions, Inc.	Unit Dose Solutions, Inc.	2026-06-29	HUMAN PRESCRIPTION DRUG LABEL
Olanzapine - Dr. Reddy's Laboratories Inc. \| Dr.Reddy's Laboratories Limited-FTO3	Dr. Reddy's Laboratories Inc. \| Dr.Reddy's Laboratories Limited-FTO3	2026-03-09	HUMAN PRESCRIPTION DRUG LABEL
Olanzapine - American Health Packaging	American Health Packaging	2025-10-20	HUMAN PRESCRIPTION DRUG LABEL
Olanzapine - Bryant Ranch Prepack	Bryant Ranch Prepack	2025-06-02	HUMAN PRESCRIPTION DRUG LABEL
Olanzapine - Quality Care Products, LLC	Quality Care Products, LLC	2022-10-26	HUMAN PRESCRIPTION DRUG LABEL
Olanzapine - A-S Medication Solutions	A-S Medication Solutions	2020-07-24	HUMAN PRESCRIPTION DRUG LABEL
Olanzapine - A-S Medication Solutions	A-S Medication Solutions	2018-08-14	HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
43598-166-01	Olanzapine	100 in 1 BOTTLE	TABLET, FILM COATED	100	13
43598-166-05	Olanzapine	500 in 1 BOTTLE	TABLET, FILM COATED	500	13
43598-166-10	Olanzapine	1000 in 1 BOTTLE	TABLET, FILM COATED	1000	13
43598-166-30	Olanzapine	30 in 1 BOTTLE	TABLET, FILM COATED	30	13
43598-166-60	Olanzapine	60 in 1 BOTTLE	TABLET, FILM COATED	60	13
43598-166-78	Olanzapine	10 in 1 CARTON	TABLET, FILM COATED	10	13
43598-166-79	Olanzapine	10 in 1 BLISTER PACK	TABLET, FILM COATED	10	13

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
43598-166	OLANZAPINE TABLET, FILM COATED [DR. REDDY'S LABORATORIES INC.]	13	Current NDC, Legacy NDC, 7 package rows	20250429_d474d5a9-d338-511d-5823-567c0a1bbf4d.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
43598-166-05	EA - Each	43598-166	3a6eaa44-fdcd-4ea7-b378-d7738a634c9e	1	2014-02-04
43598-166-30	EA - Each	43598-166	5acb32e2-8948-40ed-a1eb-8bb877d12f3c	1	2014-02-04

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
OLANZAPINE	ACTIVE INGREDIENT	N7U69T4SZR	OLANZAPINE TABLET, FILM COATED [MAJOR PHARMACEUTICALS]	7
OLANZAPINE	ACTIVE MOIETY	N7U69T4SZR	OLANZAPINE TABLET, FILM COATED [MAJOR PHARMACEUTICALS]	7
CELLULOSE, MICROCRYSTALLINE	INACTIVE INGREDIENT	OP1R32D61U	OLANZAPINE TABLET, FILM COATED [MAJOR PHARMACEUTICALS]	7
CROSPOVIDONE	INACTIVE INGREDIENT	68401960MK	OLANZAPINE TABLET, FILM COATED [MAJOR PHARMACEUTICALS]	7
HYDROXYPROPYL CELLULOSE (TYPE H)	INACTIVE INGREDIENT	RFW2ET671P	OLANZAPINE TABLET, FILM COATED [MAJOR PHARMACEUTICALS]	7
HYPROMELLOSES	INACTIVE INGREDIENT	3NXW29V3WO	OLANZAPINE TABLET, FILM COATED [MAJOR PHARMACEUTICALS]	7
LACTOSE MONOHYDRATE	INACTIVE INGREDIENT	EWQ57Q8I5X	OLANZAPINE TABLET, FILM COATED [MAJOR PHARMACEUTICALS]	7
MAGNESIUM STEARATE	INACTIVE INGREDIENT	70097M6I30	OLANZAPINE TABLET, FILM COATED [MAJOR PHARMACEUTICALS]	7
POLYETHYLENE GLYCOL 400	INACTIVE INGREDIENT	B697894SGQ	OLANZAPINE TABLET, FILM COATED [MAJOR PHARMACEUTICALS]	7
TITANIUM DIOXIDE	INACTIVE INGREDIENT	15FIX9V2JP	OLANZAPINE TABLET, FILM COATED [MAJOR PHARMACEUTICALS]	7
olanzapine	ACTIVE INGREDIENT	N7U69T4SZR	OLANZAPINE TABLET, FILM COATED [DR.REDDY'S LABORATORIES INC]	4
olanzapine	ACTIVE INGREDIENT	N7U69T4SZR	OLANZAPINE TABLET, FILM COATED [AMERICAN HEALTH PACKAGING]	4
OLANZAPINE	ACTIVE MOIETY	N7U69T4SZR	OLANZAPINE TABLET, FILM COATED [DR.REDDY'S LABORATORIES INC]	4
OLANZAPINE	ACTIVE MOIETY	N7U69T4SZR	OLANZAPINE TABLET, FILM COATED [AMERICAN HEALTH PACKAGING]	4
CELLULOSE, MICROCRYSTALLINE	INACTIVE INGREDIENT	OP1R32D61U	OLANZAPINE TABLET, FILM COATED [DR.REDDY'S LABORATORIES INC]	4
CELLULOSE, MICROCRYSTALLINE	INACTIVE INGREDIENT	OP1R32D61U	OLANZAPINE TABLET, FILM COATED [AMERICAN HEALTH PACKAGING]	4
Crospovidone	INACTIVE INGREDIENT	68401960MK	OLANZAPINE TABLET, FILM COATED [DR.REDDY'S LABORATORIES INC]	4
Crospovidone	INACTIVE INGREDIENT	68401960MK	OLANZAPINE TABLET, FILM COATED [AMERICAN HEALTH PACKAGING]	4
FD&C BLUE NO. 2	INACTIVE INGREDIENT	L06K8R7DQK	OLANZAPINE TABLET, FILM COATED [DR.REDDY'S LABORATORIES INC]	4
FD&C BLUE NO. 2	INACTIVE INGREDIENT	L06K8R7DQK	OLANZAPINE TABLET, FILM COATED [AMERICAN HEALTH PACKAGING]	4
HYDROXYPROPYL CELLULOSE (TYPE H)	INACTIVE INGREDIENT	RFW2ET671P	OLANZAPINE TABLET, FILM COATED [AMERICAN HEALTH PACKAGING]	4
Hydroxypropyl Cellulose (Type H)	INACTIVE INGREDIENT	RFW2ET671P	OLANZAPINE TABLET, FILM COATED [DR.REDDY'S LABORATORIES INC]	4
hypromelloses	INACTIVE INGREDIENT	3NXW29V3WO	OLANZAPINE TABLET, FILM COATED [AMERICAN HEALTH PACKAGING]	4
hypromelloses	INACTIVE INGREDIENT	3NXW29V3WO	OLANZAPINE TABLET, FILM COATED [DR.REDDY'S LABORATORIES INC]	4
lactose monohydrate	INACTIVE INGREDIENT	EWQ57Q8I5X	OLANZAPINE TABLET, FILM COATED [DR.REDDY'S LABORATORIES INC]	4
lactose monohydrate	INACTIVE INGREDIENT	EWQ57Q8I5X	OLANZAPINE TABLET, FILM COATED [AMERICAN HEALTH PACKAGING]	4
magnesium stearate	INACTIVE INGREDIENT	70097M6I30	OLANZAPINE TABLET, FILM COATED [AMERICAN HEALTH PACKAGING]	4
magnesium stearate	INACTIVE INGREDIENT	70097M6I30	OLANZAPINE TABLET, FILM COATED [DR.REDDY'S LABORATORIES INC]	4
POLYETHYLENE GLYCOL 400	INACTIVE INGREDIENT	B697894SGQ	OLANZAPINE TABLET, FILM COATED [DR.REDDY'S LABORATORIES INC]	4
POLYETHYLENE GLYCOL 400	INACTIVE INGREDIENT	B697894SGQ	OLANZAPINE TABLET, FILM COATED [AMERICAN HEALTH PACKAGING]	4
titanium dioxide	INACTIVE INGREDIENT	15FIX9V2JP	OLANZAPINE TABLET, FILM COATED [DR.REDDY'S LABORATORIES INC]	4
titanium dioxide	INACTIVE INGREDIENT	15FIX9V2JP	OLANZAPINE TABLET, FILM COATED [AMERICAN HEALTH PACKAGING]	4

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 30 of 113 · 2,246 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Best Choice Eye Drops Advanced Relief	DEXTRAN 70, POLYETHYLENE GLYCOL 400, POVIDONE, TETRAHYDROZOLINE HYDROCHLORIDE	Valu Merchandisers, Co.	f7491a17-8035-5a3c-e053-6294a90a615c	2025-12-30	Warnings	Exact identifier unii: B697894SGQ
Winco Advanced Relief Eye Drops	DEXTRAN 70, POLYETHYLENE GLYCOL 400, POVIDONE, TETRAHYDROZOLINE HCL	WinCo Foods, LLC	f10778c8-14fe-4852-8b73-42db502fd2bc	2025-12-30	Warnings	Exact identifier unii: B697894SGQ
Harris Teeter Eye Drops Advanced Relief	DEXTRAN 70, POLYETHYLENE GLYCOL 400, POVIDONE, TETRAHYDROZOLINE HYDROCHLORIDE	Harris Teeter, LLC	f76e2831-5c6c-7a62-e053-6294a90a937b	2025-12-30	Warnings	Exact identifier unii: B697894SGQ
CVS Gentle Tears	DEXTRAN 70, HYPROMELLOSE	CVS Pharmacy, Inc.	9b1ea0eb-c34f-6603-e053-2995a90a6a95	2025-12-30	Warnings	Exact identifier unii: 3NXW29V3WO
Foster and Thrive Lubricating Tears Lubricant Eye Drops	POLYETHYLENE GLYCOL 400, PROPYLENE GLYCOL	Strategic Sourcing Services LLC	0042337b-c22a-157a-e063-6394a90a202e	2025-12-30	Warnings	Exact identifier unii: B697894SGQ
CVS Lubricant Eye Drops Original	POLYETHYLENE GLYCOL 400, PROPYLENE GLYCOL	CVS	bb1ad35a-79ea-639f-e053-2995a90a96f3	2025-12-30	Warnings	Exact identifier unii: B697894SGQ
Foster and Thrive Advanced Relief Eye Drops	POLYETHYLENE GLYCOL 400, TETRAHYDROZOLINE HCL	Strategic Sourcing Services LLC	0019cd99-b245-2ffc-e063-6294a90a9f27	2025-12-30	Warnings	Exact identifier unii: B697894SGQ
CVS Multi-Symptom Eye Drops	POLYETHYLENE GLYCOL 400, TETRAHYDROZOLINE HCL, ZINC SULFATE	CVS Pharmacy, Inc.	be3d7855-cc66-ace8-e053-2a95a90ab8f4	2025-12-30	Warnings	Exact identifier unii: B697894SGQ
Foster and Thrive Dry Eye Relief	POLYETHYLENE GLYCOL 400	Strategic Sourcing Services LLC	0018ade9-5856-db6c-e063-6394a90a2ccf	2025-12-30	Warnings	Exact identifier unii: B697894SGQ
Foster and Thrive Long Lasting Lubricant Eye Drops	POLYETHYLENE GLYCOL 400, PROPYLENE GLYCOL	Strategic Sourcing Services LLC	00546df0-17d8-0e3c-e063-6294a90ae7b2	2025-12-30	Warnings	Exact identifier unii: B697894SGQ
Meijer Multi-Symptom Relief	POLYETHYLENE GLYCOL 400, TETRAHYDROZOLINE HCL, ZINC SULFATE	Meijer, Inc.	e7a5677a-ff33-c039-e053-2a95a90ae6c7	2025-12-30	Warnings	Exact identifier unii: B697894SGQ
Avenova Lubricant Eye Drops High Performance	POLYETHYLENE GLYCOL 400, PROPYLENE GLYCOL	NovaBay Pharmaceuticals, Inc.	cd17f037-5aa5-0ef8-e053-2a95a90a39cb	2025-12-30	Warnings	Exact identifier unii: B697894SGQ
Equate Lubricant Eye Drops	POLYETHYLENE GLYCOL 400, PROPYLENE GLYCOL	Walmart, Inc.	deebaf7f-f20d-4d7f-e053-2a95a90a4b4f	2025-12-30	Warnings	Exact identifier unii: B697894SGQ
Equate Multi-Symptom Relief Eye Drops	POLYETHYLENE GLYCOL 400,TETRAHYDROZOLINE HCL, ZINC SULFATE	Walmart, Inc.	eb8ed76b-9cd7-3636-e053-2a95a90a9583	2025-12-30	Warnings	Exact identifier unii: B697894SGQ
CorneaCare Recover Lubricant Eye Drops	POLYETHYLENE GLYCOL 400, PROPYLENE GLYCOL	CorneaCare Inc.	1fd3a5ed-8963-5c8e-e063-6394a90a6527	2025-12-30	Warnings	Exact identifier unii: B697894SGQ
Quality Choice Lubricant Eye Drops High Performance	POLYETHYLENE GLYCOL 400, PROPYLENE GLYCOL	Chain Drug Marketing Assoc., Inc.	0cd1b36a-a07a-a1db-e063-6294a90a5994	2025-12-30	Warnings	Exact identifier unii: B697894SGQ
Quality Choice Moisturizing Relief Eye Drops	DEXTRAN 70, POLYETHYLENE GLYCOL 400, POVIDONE, TETRAHYDROZOLINE HCL	Chain Drug Marketing Association, Inc.	1fb81759-5931-59c8-e063-6294a90a2277	2025-12-30	Warnings	Exact identifier unii: B697894SGQ
Quality Choice Lubricant Eye Drops Long Lasting	POLYETHYLENE GLYCOL 400, PROPYLENE GLYCOL	Chain Drug Marketing Assoc., Inc.	0cd91c45-88a2-f88c-e063-6294a90ad127	2025-12-30	Warnings	Exact identifier unii: B697894SGQ
Archies Dry Eye Relief	POLYETHYLENE GLYCOL 400, PROPYLENE GLYCOL	Archie's Remedies	07da099b-6b7f-984d-e063-6294a90a12ac	2025-12-30	Warnings	Exact identifier unii: B697894SGQ
Equaline Multi-Symptom Eye Drops	POLYETHYLENE GLYCOL 400, TETRAHYDROZOLINE HCL, ZINC SULFATE	United Natural Foods, Inc.	fe467606-6d66-b695-e053-6294a90aab5d	2025-12-30	Warnings	Exact identifier unii: B697894SGQ

Reported adverse events (FAERS/openFDA)#

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