FDA.reportPublic FDA data

Valacyclovir

Product NDC
68071-3276
11-digit product format
680713276
Labeler code
68071
Product ID
68071-3276_5033e600-1ac7-1a91-e054-00144ff8d46c
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Valacyclovir
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
NuCare Pharmaceuticals, Inc.
Application
ANDA076588
Marketing category
ANDA
Marketing start
2007-01-31
Marketing end
0000-00-00
Substance
VALACYCLOVIR HYDROCHLORIDE
Active strength
1 g/1
Pharmacologic classes
DNA Polymerase Inhibitors [MoA],Herpes Simplex Virus Nucleoside Analog DNA Polymerase Inhibitor [EPC],Herpes Zoster Virus Nucleoside Analog DNA Polymerase Inhibitor [EPC],Herpesvirus Nucleoside Analog DNA Polymerase Inhibitor [EPC],Nucleoside Analog [EXT]
NDC exclude flag
No
Listing certified through
2019-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
68071-3276-22020-05-11C16284748780-19d75b9d0-da6b-f424-e053-dadaa90a57ce5033e600-1ac6-1a91-e054-00144ff8d46c
68071-3276-42020-05-11C16284748780-19d75b9d0-da6b-f424-e053-dadaa90a57ce5033e600-1ac6-1a91-e054-00144ff8d46c
68071-3276-22020-01-31C16284748780-19d75b9d0-da6b-f424-e053-dadaa90a57ce5033e600-1ac6-1a91-e054-00144ff8d46c
68071-3276-42020-01-31C16284748780-19d75b9d0-da6b-f424-e053-dadaa90a57ce5033e600-1ac6-1a91-e054-00144ff8d46c