Home NDC 68071-4790 Acyclovir
Product NDC 68071-4790
11-digit product format 680714790
Labeler code 68071
Product ID 68071-4790_bb8e2ac0-ff50-a9c1-e053-2a95a90ab3be
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name Acyclovir
Dosage form TABLET
Route ORAL
Labeler NuCare Pharmaceuticals,Inc.
Application ANDA210401
Marketing category ANDA
Marketing start 2018-05-04
Marketing end 0000-00-00
Substance ACYCLOVIR
Active strength 800 mg/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 2022-12-31
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 68071-4790-3 68071479003 30 TABLET in 1 BOTTLE (68071-4790-3) 30 tablet 2019-03-04 0000-00-00 No No Current