Chlorzoxazone

Product NDC
42254-076
11-digit product format
422540076
Labeler code
42254
Product ID
42254-076_70cc0291-495b-4e2f-a431-ade9759ec4b7
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Chlorzoxazone
Dosage form
TABLET
Route
ORAL
Labeler
Rebel Distributors Corp
Application
ANDA089859
Marketing category
ANDA
Marketing start
2011-08-22
Marketing end
0000-00-00
Substance
CHLORZOXAZONE
Active strength
500 mg/1
Pharmacologic classes
Centrally-mediated Muscle Relaxation [PE],Muscle Relaxant [EPC]
NDC exclude flag
E
Listing certified through
2017-12-31
Current FDA listing
Historical FDA.report record

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
a7ba9d15-162f-2741-f0fc-3516be5e88bdProduct name720250114
cbf4a4f8-16cb-4546-a0cc-fd91bbe774f2Product name220240223
0a48cfb8-244e-463e-aa85-fd9bbbc9190aProduct name220200224

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
42254-076-07Chlorzoxazone7 in 1 BOTTLE, PLASTICTABLET73
42254-076-30Chlorzoxazone30 in 1 BOTTLE, PLASTICTABLET303
42254-076-40Chlorzoxazone40 in 1 BOTTLE, PLASTICTABLET403
42254-076-60Chlorzoxazone60 in 1 BOTTLE, PLASTICTABLET603
42254-076-90Chlorzoxazone90 in 1 BOTTLE, PLASTICTABLET903

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
42254-076-07EA - Each42254-0766e510216-3086-4370-b31d-88e0e4850c5012012-07-24
42254-076-30EA - Each42254-076dac224e0-2537-4237-b031-0351340bb87b12013-02-13
42254-076-40EA - Each42254-0765bbd772a-a5c3-4816-9239-defc7b85d6e212013-02-13
42254-076-60EA - Each42254-076e5405c7a-b898-418a-b436-2c12d38106cc12013-03-03
42254-076-90EA - Each42254-076b0308b91-87ad-453a-8d58-3cca5645878a12012-07-24

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
CHLORZOXAZONEACTIVE INGREDIENTH0DE420U8GCHLORZOXAZONE TABLET [REBEL DISTRIBUTORS CORP]3
CHLORZOXAZONEACTIVE MOIETYH0DE420U8GCHLORZOXAZONE TABLET [REBEL DISTRIBUTORS CORP]3
CELLULOSE, MICROCRYSTALLINEINACTIVE INGREDIENTOP1R32D61UCHLORZOXAZONE TABLET [REBEL DISTRIBUTORS CORP]3
DOCUSATE SODIUMINACTIVE INGREDIENTF05Q2T2JA0CHLORZOXAZONE TABLET [REBEL DISTRIBUTORS CORP]3
LACTOSE MONOHYDRATEINACTIVE INGREDIENTEWQ57Q8I5XCHLORZOXAZONE TABLET [REBEL DISTRIBUTORS CORP]3
MAGNESIUM STEARATEINACTIVE INGREDIENT70097M6I30CHLORZOXAZONE TABLET [REBEL DISTRIBUTORS CORP]3
SODIUM BENZOATEINACTIVE INGREDIENTOJ245FE5EUCHLORZOXAZONE TABLET [REBEL DISTRIBUTORS CORP]3
SODIUM STARCH GLYCOLATE TYPE A POTATOINACTIVE INGREDIENT5856J3G2A2CHLORZOXAZONE TABLET [REBEL DISTRIBUTORS CORP]3
STARCH, CORNINACTIVE INGREDIENTO8232NY3SJCHLORZOXAZONE TABLET [REBEL DISTRIBUTORS CORP]3

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
42254-076CHLORZOXAZONE TABLET [REBEL DISTRIBUTORS CORP]3Legacy NDC, 5 package rows20130221_9437b8ac-4f0e-4e5d-b699-23c492bf28ab.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
197502chlorzoxazone 500 MG Oral TabletPSN9437b8ac-4f0e-4e5d-b699-23c492bf28ab3
197502chlorzoxazone 500 MG Oral TabletSCD9437b8ac-4f0e-4e5d-b699-23c492bf28ab3

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionStatus
42254-076-07422540076077 in 1 BOTTLE, PLASTICHistorical
42254-076-304225400763030 in 1 BOTTLE, PLASTICHistorical
42254-076-404225400764040 in 1 BOTTLE, PLASTICHistorical
42254-076-604225400766060 in 1 BOTTLE, PLASTICHistorical
42254-076-904225400769090 in 1 BOTTLE, PLASTICHistorical