NDC 21695-021 - 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: 21695-021
Package NDCs from labels: 21695-021-15, 21695-021-20, 21695-021-21, 21695-021-30, 21695-021-42, 21695-021-60, 21695-021-90, 21695-021-72
Manufacturer: Rebel Distributors Corp.
Effective date: 2009-12-01
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
Carisoprodol - Rebel Distributors Corp.	Rebel Distributors Corp.	2009-12-01	HUMAN PRESCRIPTION DRUG LABEL WITH HIGHLIGHTS

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
21695-021-15	Carisoprodol	15 in 1 BOTTLE, PLASTIC	TABLET	15	2
21695-021-20	Carisoprodol	20 in 1 BOTTLE, PLASTIC	TABLET	20	2
21695-021-21	Carisoprodol	21 in 1 BOTTLE, PLASTIC	TABLET	21	2
21695-021-30	Carisoprodol	30 in 1 BOTTLE, PLASTIC	TABLET	30	2
21695-021-42	Carisoprodol	42 in 1 BOTTLE, PLASTIC	TABLET	42	2
21695-021-60	Carisoprodol	60 in 1 BOTTLE, PLASTIC	TABLET	60	2
21695-021-72	Carisoprodol	120 in 1 BOTTLE, PLASTIC	TABLET	120	2
21695-021-90	Carisoprodol	90 in 1 BOTTLE, PLASTIC	TABLET	90	2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
21695-021	CARISOPRODOL TABLET [REBEL DISTRIBUTORS CORP.]	2	8 package rows	20100212_f26dfb00-c55e-4cac-bc15-4f608e78a372.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
21695-021-15	EA - Each	21695-021	ef1e8535-78b4-4fd9-9ce5-9fe8cfc5acf8	1	2013-02-13
21695-021-20	EA - Each	21695-021	2ea95db7-c6e7-4a6f-a0c4-7bbc001187b9	1	2013-02-13
21695-021-21	EA - Each	21695-021	64a7c476-3209-422c-bce3-7649e7b830c3	1	2013-02-13
21695-021-30	EA - Each	21695-021	fd7a08ce-fb20-4703-b83b-1bbe7832e69e	1	2013-02-13
21695-021-42	EA - Each	21695-021	9bd85dc0-4e3a-49f1-8838-219dffbac18c	1	2013-02-13
21695-021-60	EA - Each	21695-021	ab34678d-5798-4b8b-9b76-83dc104e590a	1	2013-02-19
21695-021-72	EA - Each	21695-021	dce765cd-410e-4d6b-9433-49aa377ccdd8	1	2013-02-13
21695-021-90	EA - Each	21695-021	9db44539-50bd-4e8d-9737-959b224a7c6a	1	2013-02-13

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
CARISOPRODOL	ACTIVE INGREDIENT	21925K482H	CARISOPRODOL TABLET [REBEL DISTRIBUTORS CORP.]	2
CARISOPRODOL	ACTIVE MOIETY	21925K482H	CARISOPRODOL TABLET [REBEL DISTRIBUTORS CORP.]	2
CELLULOSE, MICROCRYSTALLINE	INACTIVE INGREDIENT	OP1R32D61U	CARISOPRODOL TABLET [REBEL DISTRIBUTORS CORP.]	2
CROSCARMELLOSE SODIUM	INACTIVE INGREDIENT	M28OL1HH48	CARISOPRODOL TABLET [REBEL DISTRIBUTORS CORP.]	2
HYPROMELLOSE	INACTIVE INGREDIENT	3NXW29V3WO	CARISOPRODOL TABLET [REBEL DISTRIBUTORS CORP.]	2
MAGNESIUM STEARATE	INACTIVE INGREDIENT	70097M6I30	CARISOPRODOL TABLET [REBEL DISTRIBUTORS CORP.]	2

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	Vensun Pharmaceuticals, Inc.	7c6015ad-2158-400d-8c22-585ab277ea49	2018-11-08	Warnings, Adverse reactions	Exact identifier rxcui: 197446 unii: 21925K482H
15f1e38f-9b47-4567-a84f-84f3b7ef11ec			f26dfb00-c55e-4cac-bc15-4f608e78a372	2009-12-01	Warnings, Adverse reactions	Exact identifier spl id: 15f1e38f-9b47-4567-a84f-84f3b7ef11ec spl set id: f26dfb00-c55e-4cac-bc15-4f608e78a372

Reported adverse events (FAERS/openFDA)#

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