CARISOPRODOL

Product NDC
61919-039
11-digit product format
619190039
Labeler code
61919
Product ID
61919-039_9e2516b3-d57e-44a7-83b4-fa7512d56a1d
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
CARISOPRODOL
Dosage form
TABLET
Route
ORAL
Labeler
Direct Rx
Application
ANDA040755
Marketing category
ANDA
Marketing start
2014-01-01
Marketing end
0000-00-00
Substance
CARISOPRODOL
Active strength
350 mg/1
Pharmacologic classes
Centrally-mediated Muscle Relaxation [PE],Muscle Relaxant [EPC]
DEA schedule
CIV
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
780d53a1-1665-e26e-d112-85333c0c8a2eProduct name520220516
2a21311a-89e2-0e83-2ebd-117f9798b2b2Product name120140508
9007e8a7-ff50-f9b9-7945-f2a1deadd94eProduct name120140508

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
61919-039-20CARISOPRODOL20 in 1 BOTTLETABLET202
61919-039-30CARISOPRODOL30 in 1 BOTTLETABLET302
61919-039-40CARISOPRODOL40 in 1 BOTTLETABLET402
61919-039-60CARISOPRODOL60 in 1 BOTTLETABLET602
61919-039-72CARISOPRODOL120 in 1 BOTTLETABLET1202
61919-039-90CARISOPRODOL90 in 1 BOTTLETABLET902

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
61919-039-20EA - Each61919-039deccc464-6577-4d5a-929e-7e10ba75ffab12015-10-02
61919-039-30EA - Each61919-0394cc298eb-cea1-4ff3-82b4-6f42a13582f212014-05-02
61919-039-40EA - Each61919-039daaa80b2-ce5f-4a9d-b431-2116ce7492d212015-07-20
61919-039-60EA - Each61919-0391587bc5e-c875-451a-9e15-01fb2f7b083e12014-05-02
61919-039-72EA - Each61919-039e5005cfb-bbaa-4585-a7eb-0d206011391012015-10-02
61919-039-90EA - Each61919-039bbae79bd-2870-4959-81e1-78aa1d09dbe812014-05-02

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
CARISOPRODOLACTIVE INGREDIENT21925K482HCARISOPRODOL TABLET [DIRECT RX]2
CARISOPRODOLACTIVE MOIETY21925K482HCARISOPRODOL TABLET [DIRECT RX]2
CELLULOSE, MICROCRYSTALLINEINACTIVE INGREDIENTOP1R32D61UCARISOPRODOL TABLET [DIRECT RX]2
CROSCARMELLOSE SODIUMINACTIVE INGREDIENTM28OL1HH48CARISOPRODOL TABLET [DIRECT RX]2
LACTOSE MONOHYDRATEINACTIVE INGREDIENTEWQ57Q8I5XCARISOPRODOL TABLET [DIRECT RX]2
MAGNESIUM STEARATEINACTIVE INGREDIENT70097M6I30CARISOPRODOL TABLET [DIRECT RX]2
POVIDONE K30INACTIVE INGREDIENTU725QWY32XCARISOPRODOL TABLET [DIRECT RX]2
STARCH, CORNINACTIVE INGREDIENTO8232NY3SJCARISOPRODOL TABLET [DIRECT RX]2
TALCINACTIVE INGREDIENT7SEV7J4R1UCARISOPRODOL TABLET [DIRECT RX]2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
61919-039CARISOPRODOL TABLET [DIRECT RX]2Legacy NDC, 6 package rows20150625_7739f2c1-9698-4a64-8d81-ef38b3ed005e.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
197446carisoprodol 350 MG Oral TabletPSN7739f2c1-9698-4a64-8d81-ef38b3ed005e2
197446carisoprodol 350 MG Oral TabletSCD7739f2c1-9698-4a64-8d81-ef38b3ed005e2

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionStatus
61919-039-206191900392020 in 1 BOTTLEHistorical
61919-039-306191900393030 in 1 BOTTLEHistorical
61919-039-406191900394040 in 1 BOTTLEHistorical
61919-039-606191900396060 in 1 BOTTLEHistorical
61919-039-7261919003972120 in 1 BOTTLEHistorical
61919-039-906191900399090 in 1 BOTTLEHistorical