NDC 49999-064-40 - Carisoprodol

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: 49999-064
Requested NDC: 49999-064-40
Package NDCs from labels: 49999-064-01, 49999-064-40
Manufacturer: Lake Erie Medical DBA Quality Care Products LLC
Effective date: 2017-02-13
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
Carisoprodol - Lake Erie Medical DBA Quality Care Products LLC	Lake Erie Medical DBA Quality Care Products LLC	2017-02-13	HUMAN PRESCRIPTION DRUG LABEL
National Council for Prescription Drug Programs indexing - billing unit	National Council for Prescription Drug Programs	2012-07-24	Indexing - Billing Unit

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
49999-064-01	2025-01-14	C162847	48780-1	9d75b9d1-0567-f424-e053-dadaa90a57ce	These highlights do not include all the information needed to use Carisoprodol Tablets, USP safely and effectively. See full prescribing information for Carisoprodol Tablets, USP. Carisoprodol Tablets for Oral use Initial U.S. Approval: 1959
49999-064-01	2020-01-31	C162847	48780-1	9d75b9d1-0567-f424-e053-dadaa90a57ce	These highlights do not include all the information needed to use Carisoprodol Tablets, USP safely and effectively. See full prescribing information for Carisoprodol Tablets, USP. Carisoprodol Tablets for Oral use Initial U.S. Approval: 1959

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
49999-064-00	EA - Each	49999-064	7a154686-49fe-4b4c-90e8-f59ddb57bc6d	1	2012-07-24
49999-064-01	EA - Each	49999-064	12ed0f6d-bb57-4c97-abf7-abe1ee7c39dc	1	2012-07-24
49999-064-10	EA - Each	49999-064	068376aa-64d2-4758-a24b-5cfe085cf568	1	2012-07-24
49999-064-14	EA - Each	49999-064	6eb5aa91-a9d1-4422-8ce5-18ce5c77e283	1	2012-07-24
49999-064-15	EA - Each	49999-064	dd593dd5-f38f-4e3b-bed2-8ee5f957b5a3	1	2012-07-24
49999-064-20	EA - Each	49999-064	f484b786-97a7-489a-ae4b-2624fcb0ffac	1	2012-07-24
49999-064-30	EA - Each	49999-064	f7db62b4-9313-4e14-b2e4-89c73af823ef	1	2012-07-24
49999-064-40	EA - Each	49999-064	fbcae89a-4031-49da-ae75-54db2ad24d85	1	2012-07-24
49999-064-50	EA - Each	49999-064	94adb7a2-b3f8-4b0a-b74e-e81c686417c7	1	2012-07-24
49999-064-90	EA - Each	49999-064	f0ef7c65-e0c9-4c6a-8a26-e3329e0a1613	1	2012-07-24

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 5 of 5 · 82 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
CARISOPRODOL	CARISOPRODOL	Proficient Rx LP	efd7a0b4-5ec5-4929-a4cb-7d207171eed6	2019-10-01	Warnings, Adverse reactions	Exact identifier unii: 21925K482H
CARISOPRODOL	CARISOPRODOL	Vensun Pharmaceuticals, Inc.	7c6015ad-2158-400d-8c22-585ab277ea49	2018-11-08	Warnings, Adverse reactions	Exact identifier unii: 21925K482H

Reported adverse events (FAERS/openFDA)#

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