balsalazide disodium

Product NDC
68682-750
11-digit product format
686820750
Labeler code
68682
Product ID
68682-750_00adff93-53db-4332-b772-bb0b7a132ddd
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
balsalazide disodium
Dosage form
CAPSULE
Route
ORAL
Labeler
Oceanside Pharmaceuticals
Application
NDA020610
Marketing category
NDA AUTHORIZED GENERIC
Marketing start
2000-07-18
Marketing end
0000-00-00
Substance
BALSALAZIDE DISODIUM
Active strength
750 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
68682-750-02EA - Each68682-750fc6ea3d5-d4c4-4600-a777-610ef2fc15ca12015-12-02

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
68682-750-0268682075002280 CAPSULE in 1 BOTTLE (68682-750-02) 280 capsule2000-07-180000-00-00NoNoCurrent