Home NDC 64679-153 VALACYCLOVIR HYDROCHLORIDE
Product NDC 64679-153
11-digit product format 646790153
Labeler code 64679
Product ID 64679-153_b7781590-447c-b37f-e053-2995a90a556f
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name VALACYCLOVIR HYDROCHLORIDE
Dosage form TABLET, FILM COATED
Route ORAL
Labeler Wockhardt USA LLC.
Application ANDA090216
Marketing category ANDA
Marketing start 2010-05-24
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 2021-12-31
Current FDA listing Historical FDA.report record FDA-Initiated Inactive NDC Indexing# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 64679-153-01 64679015301 21 TABLET, FILM COATED in 1 BOTTLE (64679-153-01) 2010-05-24 0000-00-00 No No Current 64679-153-02 64679015302 30 TABLET, FILM COATED in 1 BOTTLE (64679-153-02) 2010-05-24 0000-00-00 No No Current 64679-153-03 64679015303 90 TABLET, FILM COATED in 1 BOTTLE (64679-153-03) 2010-05-24 0000-00-00 No No Current 64679-153-04 64679015304 500 TABLET, FILM COATED in 1 BOTTLE (64679-153-04) 2010-05-24 0000-00-00 No No Current 64679-153-05 64679015305 10 BLISTER PACK in 1 CARTON (64679-153-05) > 10 TABLET, FILM COATED in 1 BLISTER PACK 10 blister pack 2010-05-24 0000-00-00 No No Current 64679-153-06 64679015306 250 TABLET, FILM COATED in 1 BOTTLE (64679-153-06) 2010-05-24 0000-00-00 No No Current