NDC 60505-0102-01 - 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: 60505-0102
Requested NDC: 60505-0102-01
Package NDCs from labels: 60505-0102-1, 60505-0102-2, 60505-0102-01
Manufacturer: Apotex Corp. | Apotex Inc.
Effective date: 2026-09-11
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	Apotex Corp. \| Apotex Inc.	2026-09-11	HUMAN PRESCRIPTION DRUG LABEL
ETODOLAC TABLETS, USP 400 mg and 500 mg Rx only	REMEDYREPACK INC.	2026-06-09	HUMAN PRESCRIPTION DRUG LABEL
ETODOLAC TABLETS, USP 500 mg Rx only	PD-Rx Pharmaceuticals, Inc.	2026-05-05	HUMAN PRESCRIPTION DRUG LABEL
Etodolac - Bryant Ranch Prepack	Bryant Ranch Prepack	2024-09-05	HUMAN PRESCRIPTION DRUG LABEL
ETODOLAC TABLETS, USP 400 mg and 500 mg Rx only	Medsource Pharmaceuticals \| Apotex Inc.	2024-03-05	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	2022-11-01	HUMAN PRESCRIPTION DRUG LABEL
Etodolac - Quality Care Products, LLC	Quality Care Products, LLC	2022-08-01	HUMAN PRESCRIPTION DRUG LABEL
ETODOLAC - DIRECT RX	DIRECT RX	2020-01-20	HUMAN PRESCRIPTION DRUG LABEL
ETODOLAC TABLETS, USP 400 mg and 500 mg Rx only	Preferred Pharmaceuticals Inc.	2019-09-16	HUMAN PRESCRIPTION DRUG LABEL
ETODOLAC - DIRECT RX	DIRECT RX	2019-04-30	HUMAN PRESCRIPTION DRUG LABEL
Etodolac - Aidarex Pharmaceuticals LLC \| Aidarex Pharmaceuticals	Aidarex Pharmaceuticals LLC \| Aidarex Pharmaceuticals	2018-08-21	HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
60505-0102-1	Etodolac	100 in 1 BOTTLE	TABLET, FILM COATED	100		16
60505-0102-2	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
60505-0102	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
60505-0102-1	EA - Each	60505-0102	4b45057f-ad61-4cd5-9d3c-dbc1ec0f2c10	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 [DIRECT RX]	1
ETODOLAC	ACTIVE MOIETY	2M36281008	ETODOLAC TABLET, FILM COATED [DIRECT RX]	1
Cellulose, Microcrystalline	INACTIVE INGREDIENT	OP1R32D61U	ETODOLAC TABLET, FILM COATED [DIRECT RX]	1
Ferric Oxide Red	INACTIVE INGREDIENT	1K09F3G675	ETODOLAC TABLET, FILM COATED [DIRECT RX]	1
Ferric Oxide Yellow	INACTIVE INGREDIENT	EX438O2MRT	ETODOLAC TABLET, FILM COATED [DIRECT RX]	1
Hypromelloses	INACTIVE INGREDIENT	3NXW29V3WO	ETODOLAC TABLET, FILM COATED [DIRECT RX]	1
Lactose Monohydrate	INACTIVE INGREDIENT	EWQ57Q8I5X	ETODOLAC TABLET, FILM COATED [DIRECT RX]	1
Magnesium Stearate	INACTIVE INGREDIENT	70097M6I30	ETODOLAC TABLET, FILM COATED [DIRECT RX]	1
Polyethylene Glycols	INACTIVE INGREDIENT	3WJQ0SDW1A	ETODOLAC TABLET, FILM COATED [DIRECT RX]	1
Povidone	INACTIVE INGREDIENT	FZ989GH94E	ETODOLAC TABLET, FILM COATED [DIRECT RX]	1
Sodium Starch Glycolate Type A Potato	INACTIVE INGREDIENT	5856J3G2A2	ETODOLAC TABLET, FILM COATED [DIRECT RX]	1
Titanium Dioxide	INACTIVE INGREDIENT	15FIX9V2JP	ETODOLAC TABLET, FILM COATED [DIRECT RX]	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 14 of 112 · 2,235 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Powder	TITANIUM DIOXIDE	Oxygen Development LLC	4d39ed7a-ca80-893c-e063-6294a90a03e7	2026-03-17	Warnings	Exact identifier unii: 15FIX9V2JP
Powder	TITANIUM DIOXIDE	Oxygen Development LLC	4d3a0a92-b0de-a1ea-e063-6294a90a8508	2026-03-17	Warnings	Exact identifier unii: 15FIX9V2JP unii: 1K09F3G675
Coral Isle SPF 50 Mineral Sunscreen	TITANIUM DIOXIDE, ZINC OXIDE	Derma Care Research Labs, LLC	0aafab44-0481-2a22-e063-6294a90abef2	2026-03-17	Warnings	Exact identifier unii: 15FIX9V2JP
SUMMER FRIDAYS SHADEDROPS BROAD SPECTRUM MINERAL MILK SUNSCREEN SPF 50	TITANIUM DIOXIDE, ZINC OXIDE	Summer Friday's LLC	4d3e982f-3489-dce2-e063-6294a90a1b9d	2026-03-17	Warnings	Exact identifier unii: 15FIX9V2JP
Sei Bella Tinted BB Moisturizing Cream	410 N	Melaleuca Inc.	2f380433-3369-9d05-e063-6394a90a6479	2026-03-17	Warnings	Exact identifier unii: 15FIX9V2JP
Sei Bella Tinted BB Moisturizing Cream	115 N	Melaleuca Inc.	2f132cc0-e8e3-35e3-e063-6394a90a4f3d	2026-03-17	Warnings	Exact identifier unii: 15FIX9V2JP
Tinted Sunscreen Broad SPF30	TINTED SUNSCREEN BROAD SPF30	DOSCHER FAMILY HEALTH NP P.C.	4d4021ba-4b29-6b81-e063-6294a90a5ea7	2026-03-17	Warnings	Exact identifier unii: 15FIX9V2JP
HYDRATING TINTED MOISTURIZER SPF50	HYDRATING TINTED MOISTURIZER SPF50	NING PTE. LTD.	4cf8d3d3-eebf-2da0-e063-6294a90a7065	2026-03-14	Warnings	Exact identifier unii: 15FIX9V2JP
TINTED WATERY SUNSCREEN	TITANIUM DIOXIDE, ZINC OXIDE	KSISTERS PTE. LTD.	4ced53d0-8bfc-ff8e-e063-6294a90a9dbd	2026-03-13	Warnings	Exact identifier unii: 15FIX9V2JP
Daily Moisturizing Mineral Sunscreen	BROAD SPECTRUM SPF30	EDINA PLASTIC SURGERY,LTD.	4d056e2b-5813-da42-e063-6294a90ac519	2026-03-13	Warnings	Exact identifier unii: 15FIX9V2JP
Leader Advanced Relief Eye Drops	DEXTRAN 70, POLYETHYLENE GLYCOL 400, POVIDONE, TETRAHYDROZOLINE HCL	Cardinal Health	5c5d6c13-9b51-48f0-8627-b60b0f707fd3	2026-03-12	Warnings	Exact identifier unii: FZ989GH94E
Neutrogena Healthy Skin Liquid Makeup Broad Spectrum SPF 20 - Cool Bronze 440C	TITANIUM DIOXIDE	Kenvue Brands LLC	4c335d9c-40ca-c0ce-e063-6394a90ac20a	2026-03-11	Warnings	Exact identifier unii: 15FIX9V2JP
Etodolac	ETODOLAC	Bryant Ranch Prepack	e7a81661-28a2-40d7-8c90-786629c81e36	2026-03-09	Boxed warning, Warnings, Adverse reactions	Exact identifier rxcui: 197684 unii: 2M36281008
Artificial Tears	GLYCERIN	Preferred Pharmaceuticals Inc.	dd646c72-8f47-43c6-a734-db0dcc8cd4d1	2026-03-06	Warnings	Exact identifier unii: 3NXW29V3WO
cle de peau BEAUTE RADIANT FLUID FOUNDATION NATURAL B50	OCTINOXATE AND TITANIUM DIOXIDE	SHISEIDO AMERICAS CORPORATION	4490f968-46b6-44d2-af2d-5130b52c8861	2026-03-05	Warnings	Exact identifier unii: 15FIX9V2JP
Calamine	CALAMINE, PRAMOXINE HCL	Amazon.com Services LLC	aceb0b10-8c90-4a06-8c47-cd1a2b4676a3	2026-03-03	Warnings, Adverse reactions	Exact identifier unii: 1K09F3G675
Calamine	FERRIC OXIDE RED	Old East Main Co.	c38c77fd-abbf-4c87-a9c0-a0e21ed3f97d	2026-03-02	Warnings, Adverse reactions	Exact identifier unii: 1K09F3G675
Calamine	FERRIC OXIDE RED	Chain Drug Marketing Association	86ff4875-9007-4b7b-8f46-16cbd475d4bb	2026-02-27	Warnings, Adverse reactions	Exact identifier unii: 1K09F3G675
Calamine	CALAMINE, PRAMOXINE HCL	Chain Drug Marketing Association	6c848b98-f01c-40f2-a9aa-2af76cb370c8	2026-02-27	Warnings, Adverse reactions	Exact identifier unii: 1K09F3G675
Levico Prunus	LEVICO PRUNUS	Uriel Pharmacy Inc.	63db9374-8ee2-48cf-8799-454c95869808	2026-02-27	Warnings	Exact identifier unii: 1K09F3G675

Reported adverse events (FAERS/openFDA)#

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