Lovastatin

Product NDC
55289-881
11-digit product format
552890881
Labeler code
55289
Product ID
55289-881_dac13313-ecb9-5d37-e053-2995a90a7dac
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
lovastatin
Dosage form
TABLET
Route
ORAL
Labeler
PD-Rx Pharmaceuticals, Inc.
Application
ANDA078296
Marketing category
ANDA
Marketing start
2007-11-01
Marketing end
0000-00-00
Substance
LOVASTATIN
Active strength
20 mg/1
Pharmacologic classes
HMG-CoA Reductase Inhibitor [EPC], Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]
NDC exclude flag
No
Listing certified through
2023-12-31
Current FDA listing
Historical FDA.report record

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
dc9a5fb6-14e2-1cc8-a567-a781fd1f0212Product name120140508
f1ae760e-e8ec-b0b4-fb1b-2db7c49fcec5Product name120140508
fecc3d5d-ff9a-60ad-1a3a-6cb9b21df758Product name120140508

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
55289-881-30EA - Each55289-881f0f1ca2f-0333-4eed-a76b-90256c56826612012-07-24
55289-881-90EA - Each55289-881ab034d4c-8826-4d96-8709-14c73c317c5012014-09-03

DailyMed Socrata Ingredients#

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
55289-881LOVASTATIN TABLET [PD-RX PHARMACEUTICALS, INC.]15Legacy NDC20240315_15ca7e87-e640-4788-b3d5-a15a0e3aa034.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
55289-881-305528908813030 TABLET in 1 BOTTLE, PLASTIC (55289-881-30) 30 tablet2015-11-050000-00-00NoNoCurrent
55289-881-905528908819090 TABLET in 1 BOTTLE, PLASTIC (55289-881-90) 90 tablet2015-11-050000-00-00NoNoCurrent