Alendronate Sodium

Product NDC
60429-056
11-digit product format
604290056
Labeler code
60429
Product ID
60429-056_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
70 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
60429-056-72EA - Each60429-05664573918-64c5-4d35-8dfb-898b25bc06c012015-06-09
60429-056-74EA - Each60429-05632a5b979-796c-4c02-9d6c-38df93ecb11912015-06-09