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 61 of 111 · 2,218 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
toty Ilumina CC Creamy Compact Refill 1C	TITANIUM DIOXIDE	Chipican LLC	f0596830-77ed-11f0-e053-2995a90a8ff5	2025-09-29	Warnings	Exact identifier unii: 15FIX9V2JP
U V-Lamp Shield Mani-Sunscreen	ZINC OXIDE, TITANIUM DIOXIDE	GUANGZHOU SAWEILAN IMPORT & EXPORT TRADING CO., LTD	3fe7e1c3-e6cd-1420-e063-6394a90a4138	2025-09-28	Warnings	Exact identifier unii: 15FIX9V2JP
Smooth Even Glow	TINTED SUNSCREEN BROAD SPF30	SKNVcare, LLC	3fa48151-fcb9-3d35-e063-6394a90a2eb6	2025-09-25	Warnings	Exact identifier unii: 15FIX9V2JP
SUN BUFF SPF 30 MINERAL SUNSCREEN	ZINC OXIDE/TITANIUM DIOXIDE	SPF Ventures, LLC	3f874062-ebab-8993-e063-6294a90abfc5	2025-09-24	Warnings	Exact identifier unii: 15FIX9V2JP
ERBORIAN CC RED CORRECT	ERBORIAN CC RED CORRECT SPF 25- OCTINOXATE, OCTISALATE, TITANIUM DIOXIDE, ZINC OXIDE CREAM	Kolmask Co., Ld.	09ca2d4b-e0c2-9961-e063-6394a90aa82e	2025-09-18		Exact identifier unii: 15FIX9V2JP
ELROEL Pang Pang Sun Cushion Plus	ZINC OXIDE, TITANIUM DIOXIDE, OCTINOXATE, OCTISALATE	MONOGLOT HOLDINGS Inc.	5ffaad65-f0b2-416a-b0a3-b92e880641e4	2025-09-18	Warnings	Exact identifier unii: 15FIX9V2JP
CVS SPF 50 Face Sunscreen	TITANIUM DIOXIDE, ZINC OXIDE	CVS	26a69a47-947a-a478-e063-6394a90aa468	2025-09-16	Warnings	Exact identifier unii: 15FIX9V2JP
Olanzapine	OLANZAPINE	Coupler LLC	3ed78a7d-4014-d280-e063-6294a90a8ee9	2025-09-15	Boxed warning, Warnings, Adverse reactions	Exact identifier rxcui: 314154 unii: N7U69T4SZR
Dry eye relief	POLYETHYLENE GLYCOL AND PROPYLENE GLYCOL	CARDINAL HEALTH 110, LLC. DBA LEADER	f8da3af5-9172-4023-be82-0fd5bd891616	2025-09-12	Warnings	Exact identifier unii: B697894SGQ
sunscreen	TITANIUM DIOXIDE(NANO)	Mingyu (guangdong) Cosmetics Technology Co., Ltd	3e6fe9f3-486b-bba7-e063-6294a90adf37	2025-09-10	Warnings	Exact identifier unii: 15FIX9V2JP
PHOFAY Matte Sunscreen Liquid Foundation SPF 30 5	ENSULIZOLE ,HOMOSALATE ,OCTINOXATE,TITANIUM DIOXIDE	Hangzhou Jingshen Trading Co., Ltd.	3dbb07e2-971c-284d-e063-6294a90a437f	2025-09-06	Warnings	Exact identifier unii: 15FIX9V2JP
PHOFAY Matte Sunscreen Liquid Foundation SPF 30 6	ENSULIZOLE,HOMOSALATE ,OCTINOXATE ,TITANIUM DIOXIDE	Hangzhou Jingshen Trading Co., Ltd.	3e069cb2-c4c5-abf5-e063-6394a90a56b0	2025-09-06	Warnings	Exact identifier unii: 15FIX9V2JP
Powder	TITANIUM DIOXIDE	Oxygen Development LLC	08b52f29-c1a0-c673-e063-6294a90a9a7a	2025-09-05	Warnings	Exact identifier unii: 15FIX9V2JP
Powder	TITANIUM DIOXIDE	Oxygen Development LLC	08b8003f-40be-3380-e063-6294a90a4f6b	2025-09-05	Warnings	Exact identifier unii: 15FIX9V2JP
Olanzapine	OLANZAPINE	Preferred Pharmaceuticals Inc.	cfc0f187-d3ff-4bbb-9129-0e94c6eda0ee	2025-09-05	Boxed warning, Warnings, Adverse reactions	Exact identifier application number: ANDA076255 rxcui: 200034 unii: N7U69T4SZR
PHOFAY Matte Sunscreen Liquid Foundation SPF 30, 1	ENSULIZOLE, HOMOSALATE, OCTINOXATE, TITANIUM DIOXIDE	Hangzhou Jingshen Trading Co., Ltd.	18130858-429c-4ed4-a75b-5bc014481250	2025-09-04	Warnings	Exact identifier unii: 15FIX9V2JP
Dolce and Gabbana Everlast Foundation SPF 20 38C Deep	OCTISALATE, OCTOCRYLENE, TITANIUM DIOXIDE, ZINC OXIDE	Dolce & Gabbana Beauty S.R.L	0358a87d-8002-4f3e-851a-3a582d356edf	2025-09-03	Warnings	Exact identifier unii: 15FIX9V2JP
Dolce and Gabbana Everlast Foundation SPF 20 39N Deep	OCTISALATE, OCTOCRYLENE, TITANIUM DIOXIDE, ZINC OXIDE	Dolce & Gabbana Beauty S.R.L	34dfc4c5-44f7-4531-97ba-8846ebe14724	2025-09-03	Warnings	Exact identifier unii: 15FIX9V2JP
Dolce and Gabbana Everlast Foundation SPF 20 40C Deep	OCTISALATE, OCTOCRYLENE, TITANIUM DIOXIDE, ZINC OXIDE	Dolce & Gabbana Beauty S.R.L	cf4b6f45-d4ae-4665-87b4-c5af4910befa	2025-09-03	Warnings	Exact identifier unii: 15FIX9V2JP
Pure6 ManiShield Hand Screen	ZINC OXIDE, TITANIUM DIOXIDE	GUANGZHOU SAWEILAN IMPORT & EXPORT TRADING CO., LTD	3abcb6ba-1de8-55e7-e063-6294a90aecf1	2025-09-02	Warnings	Exact identifier unii: 15FIX9V2JP

Reported adverse events (FAERS/openFDA)#

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