Carisoprodol

Product NDC
70518-2618
11-digit product format
705182618
Labeler code
70518
Product ID
70518-2618_d6ab3dcb-e9e2-f320-e053-2a95a90af55a
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Carisoprodol
Dosage form
TABLET
Route
ORAL
Labeler
REMEDYREPACK INC.
Application
ANDA205085
Marketing category
ANDA
Marketing start
2020-03-09
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
No
Listing certified through
2023-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
70518-2618-0EA - Each70518-26182427a0fe-6408-4d67-8236-f29d080ac16c12024-05-16
70518-2618-1EA - Each70518-2618e75e554c-e102-4367-b36d-3c1e1df967c612024-05-16

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
70518-2618CARISOPRODOL TABLET [REMEDYREPACK INC.]4Legacy NDC20220129_627af1a3-1f34-463e-9950-f7cb65347b60.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
70518-2618-07051826180090 TABLET in 1 BOTTLE, PLASTIC (70518-2618-0) 90 tablet2020-03-090000-00-00NoNoCurrent
70518-2618-17051826180160 TABLET in 1 BOTTLE, PLASTIC (70518-2618-1) 60 tablet2020-03-090000-00-00NoNoCurrent