Rosuvastatin calcium

Product NDC
71205-077
11-digit product format
712050077
Labeler code
71205
Product ID
71205-077_646857c5-dccd-4437-93f0-6b3c7529718f
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Rosuvastatin calcium
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Proficient Rx LP
Application
ANDA079171
Marketing category
ANDA
Marketing start
2016-07-19
Marketing end
0000-00-00
Substance
ROSUVASTATIN CALCIUM
Active strength
20 mg/1
Pharmacologic classes
HMG-CoA Reductase Inhibitor [EPC],Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]
NDC exclude flag
No
Listing certified through
2020-12-31
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
71205-077-30EA - Each71205-0779871c501-86a7-42bd-8ae0-1263b7208c4512018-10-11

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71205-077ROSUVASTATIN CALCIUM TABLET, FILM COATED [PROFICIENT RX LP]3Legacy NDC20191030_32747a7a-450d-4161-87b0-0ca4bdc73ef7.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
71205-077-307120500773030 TABLET, FILM COATED in 1 BOTTLE (71205-077-30) 2018-08-010000-00-00NoNoCurrent
71205-077-607120500776060 TABLET, FILM COATED in 1 BOTTLE (71205-077-60) 2018-08-010000-00-00NoNoCurrent
71205-077-907120500779090 TABLET, FILM COATED in 1 BOTTLE (71205-077-90) 2018-08-010000-00-00NoNoCurrent