sumatriptan succinate

Product NDC
42023-121
11-digit product format
420230121
Labeler code
42023
Product ID
42023-121_602f8636-913b-4686-9f3f-b625b44b7a89
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
sumatriptan succinate
Dosage form
INJECTION
Route
SUBCUTANEOUS
Labeler
JHP Pharmaceuticals LLC
Application
ANDA077871
Marketing category
ANDA
Marketing start
2009-08-06
Marketing end
0000-00-00
Substance
SUMATRIPTAN SUCCINATE
Active strength
6 mg/.5mL
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
2018-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
42023-121-052025-02-01C16284748780-19d75b9d0-a1e0-f424-e053-dadaa90a57ce05adc16c-4c2b-46f0-b810-bb18d4106dc5
42023-121-052020-01-31C16284748780-19d75b9d0-a1e0-f424-e053-dadaa90a57ce05adc16c-4c2b-46f0-b810-bb18d4106dc5

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
42023-121-05ML - Milliliter42023-121c43467ae-2e8d-48b6-9efd-a43c63703f4b12012-07-24