NDC 60505-0041-01 - Etodolac

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: 60505-0041
Requested NDC: 60505-0041-01
Package NDCs from labels: 60505-0041-1, 60505-0041-2, 60505-0041-01
Manufacturer: REMEDYREPACK INC.
Effective date: 2026-09-16
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
ETODOLAC TABLETS, USP 400 mg and 500 mg Rx only	REMEDYREPACK INC.	2026-09-16	HUMAN PRESCRIPTION DRUG LABEL
ETODOLAC TABLETS, USP 400 mg and 500 mg Rx only	Apotex Corp. \| Apotex Inc.	2026-09-11	HUMAN PRESCRIPTION DRUG LABEL
Etodolac - St. Mary’s Medical Park Pharmacy	St. Mary’s Medical Park Pharmacy	2026-06-25	HUMAN PRESCRIPTION DRUG LABEL
ETODOLAC TABLETS, USP 400 mg Rx only	PD-Rx Pharmaceuticals, Inc.	2026-05-22	HUMAN PRESCRIPTION DRUG LABEL
ETODOLAC TABLETS, USP 400 mg Rx only	PD-Rx Pharmaceuticals, Inc.	2026-04-29	HUMAN PRESCRIPTION DRUG LABEL
ETODOLAC TABLETS, USP 400 mg Rx only	PD-Rx Pharmaceuticals, Inc.	2025-12-16	HUMAN PRESCRIPTION DRUG LABEL
Etodolac - Bryant Ranch Prepack	Bryant Ranch Prepack	2025-11-14	HUMAN PRESCRIPTION DRUG LABEL
ETODOLAC TABLETS, USP 400 mg and 500 mg Rx only	Preferred Pharmaceuticals Inc.	2025-03-24	HUMAN PRESCRIPTION DRUG LABEL
Etodolac - Advanced Rx Pharmacy of Tennessee, LLC	Advanced Rx Pharmacy of Tennessee, LLC	2024-12-31	HUMAN PRESCRIPTION DRUG LABEL
ETODOLAC TABLETS, USP 400 mg and 500 mg Rx only	RPK Pharmaceuticals, Inc.	2024-12-19	HUMAN PRESCRIPTION DRUG LABEL
Etodolac - Quality Care Products LLC	Quality Care Products LLC	2024-12-17	HUMAN PRESCRIPTION DRUG LABEL
Etodolac - Bryant Ranch Prepack	Bryant Ranch Prepack	2024-09-05	HUMAN PRESCRIPTION DRUG LABEL
Etodolac - Aphena Pharma Solutions - Tennessee, LLC	Aphena Pharma Solutions - Tennessee, LLC	2024-03-20	HUMAN PRESCRIPTION DRUG LABEL
Etodolac - A-S Medication Solutions	A-S Medication Solutions	2023-12-10	HUMAN PRESCRIPTION DRUG LABEL
Etodolac - Proficient Rx LP	Proficient Rx LP	2023-08-01	HUMAN PRESCRIPTION DRUG LABEL
ETODOLAC - DIRECT RX	DIRECT RX	2023-04-17	HUMAN PRESCRIPTION DRUG LABEL
Etodolac - A-S Medication Solutions	A-S Medication Solutions	2023-02-04	HUMAN PRESCRIPTION DRUG LABEL
NuDroxiPAK E-400 - NuCare Pharmaceuticals,Inc.	NuCare Pharmaceuticals,Inc.	2021-05-07	HUMAN PRESCRIPTION DRUG LABEL
ETODOLAC TABLETS, USP 400 mg and 500 mg Rx only	Preferred Pharmaceuticals Inc.	2020-05-18	HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
60505-0041-1	Etodolac	100 in 1 BOTTLE	TABLET, FILM COATED	100		16
60505-0041-2	Etodolac	500 in 1 BOTTLE	TABLET, FILM COATED	500		16

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
60505-0041	ETODOLAC TABLET, FILM COATED [APOTEX CORP.]	15	Current NDC, Legacy NDC, 2 package rows	20240809_4d682f98-1e8a-4c2b-6df3-169d2ed10dc1.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
60505-0041-1	EA - Each	60505-0041	afbac5a4-38be-4949-a771-cbf64f0dcfb0	1	2012-07-24

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
ETODOLAC	ACTIVE INGREDIENT	2M36281008	ETODOLAC TABLET, FILM COATED [APOTEX CORP.]	5
ETODOLAC	ACTIVE MOIETY	2M36281008	ETODOLAC TABLET, FILM COATED [APOTEX CORP.]	5
CROSPOVIDONE	INACTIVE INGREDIENT	68401960MK	ETODOLAC TABLET, FILM COATED [APOTEX CORP.]	5
HYDROXYPROPYL CELLULOSE (TYPE H)	INACTIVE INGREDIENT	RFW2ET671P	ETODOLAC TABLET, FILM COATED [APOTEX CORP.]	5
HYPROMELLOSE 2208 (100 MPA.S)	INACTIVE INGREDIENT	B1QE5P712K	ETODOLAC TABLET, FILM COATED [APOTEX CORP.]	5
MAGNESIUM STEARATE	INACTIVE INGREDIENT	70097M6I30	ETODOLAC TABLET, FILM COATED [APOTEX CORP.]	5
METHYLCELLULOSE (100 CPS)	INACTIVE INGREDIENT	4GFU244C4J	ETODOLAC TABLET, FILM COATED [APOTEX CORP.]	5
POLYETHYLENE GLYCOL 1500	INACTIVE INGREDIENT	1212Z7S33A	ETODOLAC TABLET, FILM COATED [APOTEX CORP.]	5
TITANIUM DIOXIDE	INACTIVE INGREDIENT	15FIX9V2JP	ETODOLAC TABLET, FILM COATED [APOTEX CORP.]	5
Etodolac	ACTIVE INGREDIENT	2M36281008	ETODOLAC TABLET, FILM COATED [PD-RX PHARMACEUTICALS, INC.]	4
etodolac	ACTIVE MOIETY	2M36281008	ETODOLAC TABLET, FILM COATED [PD-RX PHARMACEUTICALS, INC.]	4
CROSPOVIDONE	INACTIVE INGREDIENT	68401960MK	ETODOLAC TABLET, FILM COATED [PD-RX PHARMACEUTICALS, INC.]	4
HYDROXYPROPYL CELLULOSE (TYPE H)	INACTIVE INGREDIENT	RFW2ET671P	ETODOLAC TABLET, FILM COATED [PD-RX PHARMACEUTICALS, INC.]	4
HYPROMELLOSES	INACTIVE INGREDIENT	3NXW29V3WO	ETODOLAC TABLET, FILM COATED [PD-RX PHARMACEUTICALS, INC.]	4
MAGNESIUM STEARATE	INACTIVE INGREDIENT	70097M6I30	ETODOLAC TABLET, FILM COATED [PD-RX PHARMACEUTICALS, INC.]	4
METHYLCELLULOSE (100 CPS)	INACTIVE INGREDIENT	4GFU244C4J	ETODOLAC TABLET, FILM COATED [PD-RX PHARMACEUTICALS, INC.]	4
POLYETHYLENE GLYCOLS	INACTIVE INGREDIENT	3WJQ0SDW1A	ETODOLAC TABLET, FILM COATED [PD-RX PHARMACEUTICALS, INC.]	4
TITANIUM DIOXIDE	INACTIVE INGREDIENT	15FIX9V2JP	ETODOLAC TABLET, FILM COATED [PD-RX PHARMACEUTICALS, INC.]	4
ETODOLAC	ACTIVE INGREDIENT	2M36281008	ETODOLAC TABLET, FILM COATED [STAT RX USA LLC]	1
ETODOLAC	ACTIVE INGREDIENT	2M36281008	ETODOLAC TABLET, FILM COATED [PREFERRED PHARMACEUTICALS INC.]	1
ETODOLAC	ACTIVE MOIETY	2M36281008	ETODOLAC TABLET, FILM COATED [PREFERRED PHARMACEUTICALS INC.]	1
ETODOLAC	ACTIVE MOIETY	2M36281008	ETODOLAC TABLET, FILM COATED [STAT RX USA LLC]	1
CROSPOVIDONE	INACTIVE INGREDIENT	68401960MK	ETODOLAC TABLET, FILM COATED [STAT RX USA LLC]	1
CROSPOVIDONE	INACTIVE INGREDIENT	68401960MK	ETODOLAC TABLET, FILM COATED [PREFERRED PHARMACEUTICALS INC.]	1
HYDROXYPROPYL CELLULOSE	INACTIVE INGREDIENT	RFW2ET671P	ETODOLAC TABLET, FILM COATED [STAT RX USA LLC]	1
HYDROXYPROPYL CELLULOSE (TYPE H)	INACTIVE INGREDIENT	RFW2ET671P	ETODOLAC TABLET, FILM COATED [PREFERRED PHARMACEUTICALS INC.]	1
HYPROMELLOSE 2208 (100 MPA.S)	INACTIVE INGREDIENT	B1QE5P712K	ETODOLAC TABLET, FILM COATED [PREFERRED PHARMACEUTICALS INC.]	1
HYPROMELLOSES	INACTIVE INGREDIENT	3NXW29V3WO	ETODOLAC TABLET, FILM COATED [STAT RX USA LLC]	1
MAGNESIUM STEARATE	INACTIVE INGREDIENT	70097M6I30	ETODOLAC TABLET, FILM COATED [STAT RX USA LLC]	1
MAGNESIUM STEARATE	INACTIVE INGREDIENT	70097M6I30	ETODOLAC TABLET, FILM COATED [PREFERRED PHARMACEUTICALS INC.]	1
METHYLCELLULOSE (100 CPS)	INACTIVE INGREDIENT	4GFU244C4J	ETODOLAC TABLET, FILM COATED [STAT RX USA LLC]	1
METHYLCELLULOSE (100 MPA.S)	INACTIVE INGREDIENT	4GFU244C4J	ETODOLAC TABLET, FILM COATED [PREFERRED PHARMACEUTICALS INC.]	1
POLYETHYLENE GLYCOL	INACTIVE INGREDIENT	3WJQ0SDW1A	ETODOLAC TABLET, FILM COATED [STAT RX USA LLC]	1
POLYETHYLENE GLYCOL 1500	INACTIVE INGREDIENT	1212Z7S33A	ETODOLAC TABLET, FILM COATED [PREFERRED PHARMACEUTICALS INC.]	1
TITANIUM DIOXIDE	INACTIVE INGREDIENT	15FIX9V2JP	ETODOLAC TABLET, FILM COATED [STAT RX USA LLC]	1
TITANIUM DIOXIDE	INACTIVE INGREDIENT	15FIX9V2JP	ETODOLAC TABLET, FILM COATED [PREFERRED PHARMACEUTICALS INC.]	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 3 of 238 · 4,744 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
MELAO Hydrating Lightweight Sunscreen	AVOBENZONE,ENSULIZOLE,HOMOSALATE,OCTISALATE,OCTOCRYLENE,TITANIUM DIOXIDE	Guangdong Aimu Biological Technology Co., Ltd	59eeaea1-d726-99f3-e063-6394a90aeea3	2026-08-26	Warnings	Exact identifier unii: 15FIX9V2JP
Careland Lidocaine Plus Menthol Pain Relieving	LIDOCAINE, MENTHOL	Planet (Anhui) Pharmaceutical Co., Ltd	0f928b5b-60f5-4a45-a409-c601eb330487	2026-08-26	Warnings	Exact identifier unii: L7T10EIP3A
PARCHE CALIENTE	CAPSAICINA AND MENTOL	DW SUPPORT LLC	59f2708e-295a-ccb3-e063-6394a90ad395	2026-08-26	Warnings	Exact identifier unii: S07O44R1ZM unii: L7T10EIP3A
KUGIG ALOE FOAMING INTIMATE WASH	INTIMATE CLEANSING FOAM	Hong Kong KangXing Centennial Management Limited	59f4d398-1186-a168-e063-6294a90ab44b	2026-08-26	Warnings	Exact identifier unii: 059QF0KO0R
Kreain Nature Soothing Cooling	KREAIN NATURE SOOTHING COOLING	WANWANG INC	59e046de-2be7-26bd-e063-6394a90a4b31	2026-08-25	Warnings	Exact identifier unii: L7T10EIP3A
Q Skin Science	SUNSCREEN	International Cosmeceuticals, Inc	59e4c3d0-ee4c-2350-e063-6394a90ac9d2	2026-08-25	Warnings	Exact identifier unii: 15FIX9V2JP
Etodolac	ETODOLAC	Bryant Ranch Prepack	ea12933b-2280-4a11-a0e3-554194c53c4d	2026-08-25	Boxed warning, Warnings, Adverse reactions	Exact identifier unii: 2M36281008
MELAO zinc stick(GREEN)	TITANIUM DIOXIDE,ZINC OXIDE,OCTOCRYLENE	Guangzhou Haishi Biological Technology Co., Ltd.	59c70c82-f7ff-9a04-e063-6294a90a7b3d	2026-08-24	Warnings	Exact identifier unii: 15FIX9V2JP
HEEL PAIN RELIEF ROLL-ON	LIDOCAINE AND MENTHOL	Guangzhou Liuquanmiao Import & Export Trade Co., Ltd.	59c7e13f-b9ea-023a-e063-6294a90a79e0	2026-08-24	Warnings	Exact identifier unii: L7T10EIP3A
KNEE PAIN RELIEF ROLL-ON	LIDOCAINE AND MENTHOL	Guangzhou Liuquanmiao Import & Export Trade Co., Ltd.	59c8b33a-7d4f-2c6e-e063-6394a90a7929	2026-08-24	Warnings	Exact identifier unii: L7T10EIP3A
Sterile Water	WATER	REMEDYREPACK INC.	5dd5d148-6e23-41de-bff5-551b2aea9598	2026-08-24	Warnings, Adverse reactions	Exact identifier unii: 059QF0KO0R
SKIN-INFUSED FOUNDATION SPF 25/ Mineral sunscreen broad Spectrum SPF 25 01	ZINC OXIDE, TITANIUM DIOXIDE	Cosmuses Cosmetics (Ningbo) Co., Ltd.	59d74e3f-e3fa-a7a9-e063-6294a90a76e5	2026-08-24	Warnings	Exact identifier unii: 15FIX9V2JP
BOTASUN SMELLING SALTS	MENTHO 15% SMELLING SALTS	Hubei Minxin Pharmaceutical Co., Ltd.	59a02fae-b413-bd93-e063-6394a90a8064	2026-08-22	Warnings	Exact identifier unii: L7T10EIP3A
JELVOXA DMSO	CAMPHOR CAPSAICIN MENTHOL	Wuhan Ruihengjie Technology Co., Ltd.	59a43e2c-d258-34b5-e063-6394a90a09bf	2026-08-22	Warnings	Exact identifier unii: S07O44R1ZM unii: L7T10EIP3A
Capsaicin 0.035 Percent	CAPSAICIN	Preferred Pharmaceuticals Inc.	0fabc025-4208-45f5-b3c2-543ae3a2df41	2026-08-21	Warnings	Exact identifier unii: S07O44R1ZM
ZYLOTROL MAXIMUM PAIN	LIDOCAINE 4%, MENTHOL 1%	Whitestone Products LLC	a80efad7-1d8b-4d8b-8c97-373174ce89ca	2026-08-21	Warnings	Exact identifier unii: L7T10EIP3A
ETERNAL SPIRIT BEAUTY PAINLESS PAIN RELIEVING	MENTHOL, CAMPHOR	Worldwide Cosmetics, Inc	3b8c2419-7a78-2731-e054-00144ff8d46c	2026-08-21	Warnings	Exact identifier unii: L7T10EIP3A
Antispetic	EUCALYPTOL, MENTHOL, METHYL SALICYLATE, THYMOL	Your Military Exchanges	d0ede39c-4b05-47c7-9c0b-9e893dcdb723	2026-08-21	Warnings, Adverse reactions	Exact identifier unii: L7T10EIP3A unii: LAV5U5022Y
Tartar control plus Antiseptic	EUCALYPTOL, MENTHOL, METHYL SALICYLATE, THYMOL	Nice-Pak Products, LLC	37be182d-16be-4edb-bccb-87c7cb5c39c2	2026-08-21	Warnings, Adverse reactions	Exact identifier unii: L7T10EIP3A unii: LAV5U5022Y
PARCHE FRIO	METHYL SALICYLATE, MENTHOL, AND CAMPHOR PATCH	DW SUPPORT LLC	5970a6f7-b273-9bb1-e063-6394a90afc79	2026-08-21	Warnings	Exact identifier unii: L7T10EIP3A unii: LAV5U5022Y

Reported adverse events (FAERS/openFDA)#

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