Tolazamide

Product NDC
55289-265
11-digit product format
552890265
Labeler code
55289
Product ID
55289-265_7b33fbac-3018-0b82-e053-2991aa0abc53
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
tolazamide
Dosage form
TABLET
Route
ORAL
Labeler
PD-Rx Pharmaceuticals, Inc.
Application
ANDA070259
Marketing category
ANDA
Marketing start
2010-01-05
Marketing end
0000-00-00
Substance
TOLAZAMIDE
Active strength
250 mg/1
Pharmacologic classes
Sulfonylurea [EPC],Sulfonylurea Compounds [CS]
NDC exclude flag
No
Listing certified through
2019-12-31
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
55289-265-90EA - Each55289-265c57793e4-8855-443a-9f0d-7a4239df290812012-07-24