Ritonavir

Product NDC
0054-0407
11-digit product format
000540407
Labeler code
0054
Product ID
0054-0407_ec8d993c-1d1e-4c8d-83d9-87f6048b1902
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Ritonavir
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
West-Ward Pharmaceuticals Corp.
Application
ANDA202573
Marketing category
ANDA
Marketing start
2018-03-20
Marketing end
0000-00-00
Substance
RITONAVIR
Active strength
100 mg/1
Pharmacologic classes
Breast Cancer Resistance Protein Inhibitors [MoA], Cytochrome P450 1A2 Inducers [MoA], Cytochrome P450 2B6 Inducers [MoA], Cytochrome P450 2C19 Inducers [MoA], Cytochrome P450 2C9 Inducers [MoA], Cytochrome P450 2D6 Inhibitors [MoA], Cytochrome P450 3A Inducers [MoA], Cytochrome P450 3A Inhibitor [EPC], Cytochrome P450 3A Inhibitors [MoA], Cytochrome P450 3A4 Inhibitors [MoA], HIV Protease Inhibitors [MoA], P-Glycoprotein Inhibitors [MoA], Protease Inhibitor [EPC], UDP Glucuronosyltransferases Inducers [MoA]
NDC exclude flag
No
Listing certified through
2023-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
0054-0407-13EA - Each0054-0407776d2475-5a3b-4082-b48f-c5ab7dda019312018-04-19

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
0054-0407-130005404071330 TABLET, FILM COATED in 1 BOTTLE (0054-0407-13) 2018-03-200000-00-00NoNoCurrent