sumatriptan succinate

Product NDC
55700-093
11-digit product format
557000093
Labeler code
55700
Product ID
55700-093_5362a2c8-74c1-45b5-bf88-a4878b4dbd54
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
sumatriptan succinate
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Lake Erie Medical DBA Quality Care Products LLC
Application
ANDA078295
Marketing category
ANDA
Marketing start
2009-08-10
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
No
Listing certified through
2022-12-31
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
55700-093-09EA - Each55700-0933d81ab4d-472e-42e3-88a8-305be48b9da912019-09-05
55700-093-30EA - Each55700-0933c593ec1-7f69-4ba0-a5e5-6b51133eb7ae12015-04-03

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
55700-093-09557000093099 TABLET, FILM COATED in 1 BLISTER PACK (55700-093-09) 2019-07-260000-00-00NoNoCurrent
55700-093-305570000933030 TABLET, FILM COATED in 1 BOTTLE (55700-093-30) 2009-08-100000-00-00NoNoCurrent