Leucovorin Calcium

Product NDC
51079-582
11-digit product format
510790582
Labeler code
51079
Product ID
51079-582_f0e61488-11f1-9fa6-e053-2995a90aedf5
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Leucovorin Calcium
Dosage form
TABLET
Route
ORAL
Labeler
Mylan institutional Inc.
Application
ANDA071199
Marketing category
ANDA
Marketing start
1997-08-27
Marketing end
2023-06-30
Substance
LEUCOVORIN CALCIUM
Active strength
25 mg/1
Pharmacologic classes
Folate Analog [EPC], Folic Acid [CS]
NDC exclude flag
No
Listing certified through
0000-00-00
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
51079-582-01EA - Each51079-5823496a72b-7182-4880-ad27-b982641c174e12012-07-24
51079-582-05EA - Each51079-582b50f91df-ca52-43fe-9ca8-28f9ea76d14112012-07-24

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
51079-582-055107905820520 BLISTER PACK in 1 CARTON (51079-582-05) > 1 TABLET in 1 BLISTER PACK (51079-582-01) 20 blister pack1997-08-270000-00-00NoNoCurrent