Exservan

Product NDC
70510-2201
11-digit product format
705102201
Labeler code
70510
Product ID
70510-2201_b0b60143-27ab-439c-b949-10ddb0e54984
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
riluzole
Dosage form
FILM
Route
ORAL
Labeler
Mitsubishi Tanabe Pharma America, Inc.
Application
NDA212640
Marketing category
NDA
Marketing start
2021-05-01
Marketing end
0000-00-00
Substance
RILUZOLE
Active strength
50 mg/1
Pharmacologic classes
Benzothiazole [EPC], Benzothiazoles [CS]
NDC exclude flag
No
Listing certified through
2023-12-31
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
70510-2201-1EA - Each70510-22010b69f8fe-0796-45ae-a049-1e49e9b2238712021-06-02
70510-2201-2EA - Each70510-2201c5bdf257-d43a-4070-a97d-3655cb7ab40412021-06-02

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
70510-2201-27051022010260 POUCH in 1 CARTON (70510-2201-2) > 1 FILM in 1 POUCH (70510-2201-1) 60 pouch2021-05-010000-00-00NoNoCurrent