Sulfasalazine

Product NDC
23155-019
11-digit product format
231550019
Labeler code
23155
Product ID
23155-019_f049e60c-96e6-2dfe-e053-2995a90a3489
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Sulfasalazine
Dosage form
TABLET
Route
ORAL
Labeler
HERITAGE PHARMACEUTICALS INC. D/B/A AVET PHARMACEUTICALS INC.
Application
ANDA080197
Marketing category
ANDA
Marketing start
1973-11-12
Marketing end
0000-00-00
Substance
SULFASALAZINE
Active strength
500 mg/1
Pharmacologic classes
Aminosalicylate [EPC], Aminosalicylic Acids [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
23155-019-01EA - Each23155-019c70daff2-13c4-4354-9be6-963140f1fa4912021-06-02

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
23155-019-0123155001901100 TABLET in 1 BOTTLE (23155-019-01) 100 tablet2021-05-070000-00-00NoNoCurrent
23155-019-0523155001905500 TABLET in 1 BOTTLE (23155-019-05) 500 tablet2021-05-070000-00-00NoNoCurrent
23155-019-10231550019101000 TABLET in 1 BOTTLE (23155-019-10) 1000 tablet2021-05-070000-00-00NoNoCurrent
23155-019-1323155001913300 TABLET in 1 BOTTLE (23155-019-13) 300 tablet2021-05-070000-00-00NoNoCurrent