NDC 0832-0038-89 - Oxybutynin Chloride

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: 0832-0038
Requested NDC: 0832-0038-89
Package NDCs from labels: 0832-0038-00, 0832-0038-50, 0832-0038-10, 0832-0038-89, 0832-0038-01
Manufacturer: Upsher-Smith Laboratories, LLC | Bora Pharmaceuticals, Inc
Effective date: 2025-12-11
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
Oxybutynin Chloride - Upsher-Smith Laboratories, LLC \| Bora Pharmaceuticals, Inc	Upsher-Smith Laboratories, LLC \| Bora Pharmaceuticals, Inc	2025-12-11	HUMAN PRESCRIPTION DRUG LABEL
Oxybutynin Chloride - RedPharm Drug, Inc.	RedPharm Drug, Inc.	2022-01-20	HUMAN PRESCRIPTION DRUG LABEL
Oxybutynin Chloride Tablets, USP	REMEDYREPACK INC.	2019-12-18	HUMAN PRESCRIPTION DRUG LABEL
Oxybutynin Chloride Tablets, USP	REMEDYREPACK INC.	2019-08-14	HUMAN PRESCRIPTION DRUG LABEL
Oxybutynin Chloride - Aidarex Pharmaceuticals LLC \| Aidarex Pharmaceuticals	Aidarex Pharmaceuticals LLC \| Aidarex Pharmaceuticals	2018-08-13	HUMAN PRESCRIPTION DRUG LABEL
Oxybutynin Chloride - A-S Medication Solutions	A-S Medication Solutions	2017-09-21	HUMAN PRESCRIPTION DRUG LABEL
Oxybutynin Chloride - Aphena Pharma Solutions - Tennessee, LLC	Aphena Pharma Solutions - Tennessee, LLC	2016-06-15	HUMAN PRESCRIPTION DRUG LABEL
Oxybutynin Chloride - State of Florida DOH Central Pharmacy	State of Florida DOH Central Pharmacy	2013-09-26	HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
0832-0038-00	Oxybutynin Chloride	100 in 1 BOTTLE	TABLET	100	17
0832-0038-01	Oxybutynin Chloride	100 in 1 CARTON	TABLET	100	17
0832-0038-10	Oxybutynin Chloride	1000 in 1 BOTTLE	TABLET	1000	17
0832-0038-50	Oxybutynin Chloride	500 in 1 BOTTLE	TABLET	500	17
0832-0038-89	Oxybutynin Chloride	1 in 1 BLISTER PACK	TABLET	1	17

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
0832-0038	OXYBUTYNIN CHLORIDE TABLET [UPSHER-SMITH LABORATORIES, LLC]	15	Current NDC, Legacy NDC, 5 package rows	20230921_3ee6835a-7a7d-49a9-8460-2f1dd270ead3.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
0832-0038-00	EA - Each	0832-0038	f3763031-4e45-4646-a8ba-3d7de1546c35	1	2012-07-24
0832-0038-01	EA - Each	0832-0038	1d2f3647-37a1-426a-948e-97432f95886d	1	2018-06-11
0832-0038-10	EA - Each	0832-0038	177cafb0-d308-4e31-89b9-4595cb6ea70e	1	2012-07-24
0832-0038-50	EA - Each	0832-0038	45fb36e1-d85b-47fb-970b-be7fd4528abb	1	2012-07-24
0832-0038-89	EA - Each	0832-0038	ebc21517-3bb5-4b5e-a6ad-415af411acff	1	2018-06-11

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
Oxybutynin Chloride	ACTIVE INGREDIENT	L9F3D9RENQ	OXYBUTYNIN CHLORIDE TABLET [UPSHER-SMITH LABORATORIES, INC.]	8
Oxybutynin	ACTIVE MOIETY	K9P6MC7092	OXYBUTYNIN CHLORIDE TABLET [UPSHER-SMITH LABORATORIES, INC.]	8
anhydrous lactose	INACTIVE INGREDIENT	3SY5LH9PMK	OXYBUTYNIN CHLORIDE TABLET [UPSHER-SMITH LABORATORIES, INC.]	8
calcium stearate	INACTIVE INGREDIENT	776XM7047L	OXYBUTYNIN CHLORIDE TABLET [UPSHER-SMITH LABORATORIES, INC.]	8
cellulose, microcrystalline	INACTIVE INGREDIENT	OP1R32D61U	OXYBUTYNIN CHLORIDE TABLET [UPSHER-SMITH LABORATORIES, INC.]	8
OXYBUTYNIN CHLORIDE	ACTIVE INGREDIENT	L9F3D9RENQ	OXYBUTYNIN CHLORIDE TABLET [STATE OF FLORIDA DOH CENTRAL PHARMACY]	1
OXYBUTYNIN	ACTIVE MOIETY	K9P6MC7092	OXYBUTYNIN CHLORIDE TABLET [STATE OF FLORIDA DOH CENTRAL PHARMACY]	1
ANHYDROUS LACTOSE	INACTIVE INGREDIENT	3SY5LH9PMK	OXYBUTYNIN CHLORIDE TABLET [STATE OF FLORIDA DOH CENTRAL PHARMACY]	1
CALCIUM STEARATE	INACTIVE INGREDIENT	776XM7047L	OXYBUTYNIN CHLORIDE TABLET [STATE OF FLORIDA DOH CENTRAL PHARMACY]	1
CELLULOSE, MICROCRYSTALLINE	INACTIVE INGREDIENT	OP1R32D61U	OXYBUTYNIN CHLORIDE TABLET [STATE OF FLORIDA DOH CENTRAL PHARMACY]	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 5 · 89 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Oxybutynin Chloride	OXYBUTYNIN CHLORIDE	PD-Rx Pharmaceuticals, Inc.	0c021aad-97a3-4404-a11e-cdd2ec731c6b	2025-03-07	Warnings, Adverse reactions	Exact identifier rxcui: 863664 unii: L9F3D9RENQ
YVTYVT MICRODERMABRASION FACIAL SCRUB	YVTYVT MICRODERMABRASION FACIAL SCRUB	Beijing JUNGE Technology Co., Ltd.	2f30fc45-42e2-c766-e063-6394a90a8d68	2025-02-28	Warnings	Exact identifier unii: OP1R32D61U
OXYBUTYNIN CHLORIDE	OXYBUTYNIN CHLORIDE	PD-Rx Pharmaceuticals, Inc.	3a319017-4e25-402e-8ba0-63b9f1eb707e	2025-02-27	Warnings, Adverse reactions	Exact identifier rxcui: 863664 unii: L9F3D9RENQ
Oxybutynin Chloride	OXYBUTYNIN CHLORIDE	Chartwell RX, LLC	d02e411b-2f34-4d08-a92a-9762cab47269	2025-02-26	Adverse reactions	Exact identifier unii: L9F3D9RENQ
Oxybutynin Chloride	OXYBUTYNIN CHLORIDE	Bryant Ranch Prepack	f92cf6d0-5f49-40e2-a4f4-8ff377cacbfb	2025-01-30	Warnings, Adverse reactions	Exact identifier rxcui: 863664 unii: L9F3D9RENQ
OXYBUTYNIN CHLORIDE	OXYBUTYNIN CHLORIDE	Redpharm Drug	fc4cfbe6-a940-41c0-e053-6294a90adb14	2025-01-23	Warnings, Adverse reactions	Exact identifier rxcui: 863664 unii: L9F3D9RENQ
OXYBUTYNIN CHLORIDE	OXYBUTYNIN CHLORIDE	direct rx	b3d6d2a8-97c4-5bad-e053-2a95a90a155d	2025-01-17	Warnings, Adverse reactions	Exact identifier rxcui: 863664 unii: L9F3D9RENQ
OXYBUTYNIN CHLORIDE	OXYBUTYNIN CHLORIDE	DIRECT RX	ada3be87-2cdd-75f7-e053-2995a90aa95b	2025-01-17	Warnings, Adverse reactions	Exact identifier unii: L9F3D9RENQ
Oxybutynin Chloride	OXYBUTYNIN CHLORIDE	Golden State Medical Supply, Inc.	6f409d7f-b064-1363-e053-2a91aa0a3a14	2024-12-23	Warnings, Adverse reactions	Exact identifier rxcui: 863664 unii: L9F3D9RENQ
Oxybutynin Chloride	OXYBUTYNIN CHLORIDE	KVK-Tech, Inc.	f99fdfe8-a980-4a72-bc99-aa2ce0bdfd86	2024-12-06	Warnings, Adverse reactions	Exact identifier rxcui: 863664 unii: L9F3D9RENQ
oxybutynin	OXYBUTYNIN	Zydus Lifesciences Limited	f405a774-bd91-4513-b7c7-c44f0596d988	2024-12-03		Exact identifier unii: L9F3D9RENQ
Oxybutynin Chloride	OXYBUTYNIN CHLORIDE	ANI Pharmaceuticals, Inc.	3b1f5585-9b33-4a96-bf33-8e6bab14bf0c	2024-11-25	Warnings, Adverse reactions	Exact identifier rxcui: 863664 unii: L9F3D9RENQ
Oxybutynin Chloride	OXYBUTYNIN CHLORIDE	Aphena Pharma Solutions - Tennessee, LLC	2425f49f-ade3-5178-e063-6294a90adfac	2024-10-10	Warnings, Adverse reactions	Exact identifier rxcui: 863664 unii: L9F3D9RENQ
Oxybutynin Chloride	OXYBUTYNIN CHLORIDE	Bryant Ranch Prepack	246d2f79-8ab5-4023-9068-1451b695ac16	2024-10-03	Warnings, Adverse reactions	Exact identifier rxcui: 863664 unii: L9F3D9RENQ
oxybutynin	OXYBUTYNIN	NCS HealthCare of KY, LLC dba Vangard Labs	ec4fd95f-16dc-4acf-b560-b67b7aaef08b	2024-09-13	Warnings, Adverse reactions	Exact identifier unii: L9F3D9RENQ
Oxybutynin Chloride	OXYBUTYNIN CHLORIDE	Teva Pharmaceuticals USA, Inc.	cb7aba8d-6913-4f57-8eb4-c6d6ff0b2a29	2024-09-02	Warnings, Adverse reactions	Exact identifier rxcui: 863664 unii: L9F3D9RENQ
Oxybutynin Chloride	OXYBUTYNIN CHLORIDE	NuCare Pharmaceuticals,Inc.	8e830697-a6d3-13ed-e053-2995a90acb11	2024-08-14	Warnings, Adverse reactions	Exact identifier rxcui: 863664 unii: L9F3D9RENQ
oxybutynin	OXYBUTYNIN	NCS HealthCare of KY, LLC dba Vangard Labs	ed10f0c9-23d6-4ded-b17f-ed474632a965	2024-08-12	Warnings, Adverse reactions	Exact identifier unii: L9F3D9RENQ
OXYBUTYNIN CHLORIDE	OXYBUTYNIN CHLORIDE	Bryant Ranch Prepack	f26e590d-956e-493b-a6ac-6056aeeaf411	2024-08-09	Warnings, Adverse reactions	Exact identifier rxcui: 863664 unii: L9F3D9RENQ
OXYBUTYNIN CHLORIDE	OXYBUTYNIN CHLORIDE	RISING PHARMA HOLDINGS, INC.	f8ed80f2-6c3d-4d7f-b761-c2447973c1f9	2024-07-03	Warnings, Adverse reactions	Exact identifier rxcui: 863664 unii: L9F3D9RENQ

Reported adverse events (FAERS/openFDA)#

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