Alendronate Sodium

Product NDC
60429-055
11-digit product format
604290055
Labeler code
60429
Product ID
60429-055_9b7cb00a-dbbe-6d0c-e053-2a95a90af1fc
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Alendronate Sodium
Dosage form
TABLET
Route
ORAL
Labeler
Golden State Medical Supply, Inc.
Application
ANDA090258
Marketing category
ANDA
Marketing start
2014-04-03
Marketing end
0000-00-00
Substance
ALENDRONATE SODIUM
Active strength
35 mg/1
Pharmacologic classes
Bisphosphonate [EPC],Diphosphonates [CS]
NDC exclude flag
No
Listing certified through
2021-12-31
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
60429-055-72EA - Each60429-055e9f704d2-3fbe-4d04-92aa-a2137e10732512015-06-09
60429-055-74EA - Each60429-0551bdc58ea-865d-4746-9b92-407bc9b5119212015-06-09