IMITREX

Product NDC
21695-154
11-digit product format
216950154
Labeler code
21695
Product ID
21695-154_a169b0c0-600f-4072-8ab7-fafc386eab80
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
sumatriptan succinate
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Rebel Distributors Corp
Application
NDA020132
Marketing category
NDA
Marketing start
2003-12-17
Marketing end
0000-00-00
Substance
SUMATRIPTAN SUCCINATE
Active strength
50 mg/1
Pharmacologic classes
Serotonin 1d Receptor Agonists [MoA],Serotonin-1b and Serotonin-1d Receptor Agonist [EPC],Serotonin 1b Receptor Agonists [MoA]
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
59adc2ba-d5f0-4a52-b35a-cc77921a79d2Product name420250724
2839c963-7eb3-970a-287f-ff1b6d381268Product name220250103
fb7ab793-2c12-4079-b100-a64f73bef25aProduct name420240712
b0cbf770-6cc3-4aa4-9158-755110c2b9f7Product name220230717
dc7c5daa-021f-40dd-b00d-63982cb2067aProduct name120230426
1e973b2d-e028-69cd-9258-4613ba80fdc5Product name320210512
08ffbcbf-26df-b99c-1dab-64fc4cfae89fProduct name520200925
3eb481d3-8b69-436f-82dd-4a66345568abProduct name120190611
816b97af-edc5-4060-aff1-b814bdbcad50Product name120190415
e76dbbc1-775d-722c-08ff-ed45e8a80defProduct name320181002
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
419aab54-5d5a-4146-9453-026d4a9991beProduct name220170525
08ffbcbf-26df-b99c-1dab-64fc4cfae89fProduct name220160823
c100f0c7-e9dd-42f4-b0a8-0d81bd2a877cProduct name120160303
49615343-b619-4365-8118-8f2ed6046e78Product name120160224
a6319377-430a-43db-82f9-30d1d9d89cf8Product name120151216
89dac932-b90a-4410-9ab1-84c53e57de25Product name120150316
f6199b09-e585-7ceb-4b09-803cf5ce1ed1Product name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
21695-154-092019-09-24C16284748780-1934fe258-48e1-48b1-e053-8cdaa90a720aIMITREX ® (sumatriptan succinate) Tablets

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
21695-154-09IMITREX9 in 1 BLISTER PACKTABLET, FILM COATED91

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
21695-154-09EA - Each21695-154212a5eb0-89cd-42d0-9fa2-90788a907aae12012-07-24

DailyMed Socrata Ingredients#

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
21695-154IMITREX (SUMATRIPTAN SUCCINATE) TABLET, FILM COATED [REBEL DISTRIBUTORS CORP]1Legacy NDC, 1 package rows20110622_a169b0c0-600f-4072-8ab7-fafc386eab80.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
209169IMITREX 50 MG Oral TabletPSNa169b0c0-600f-4072-8ab7-fafc386eab801
313161SUMAtriptan succinate 50 MG Oral TabletPSNa169b0c0-600f-4072-8ab7-fafc386eab801
209169sumatriptan 50 MG Oral Tablet [Imitrex]SBDa169b0c0-600f-4072-8ab7-fafc386eab801
313161sumatriptan 50 MG Oral TabletSCDa169b0c0-600f-4072-8ab7-fafc386eab801
209169Imitrex 50 MG (sumatriptan succinate 70 MG) Oral TabletSYa169b0c0-600f-4072-8ab7-fafc386eab801
209169Imitrex 50 MG Oral TabletSYa169b0c0-600f-4072-8ab7-fafc386eab801
313161sumatriptan 50 MG (as sumatriptan succinate 70 MG) Oral TabletSYa169b0c0-600f-4072-8ab7-fafc386eab801

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionStatus
21695-154-09216950154099 in 1 BLISTER PACKHistorical