Home NDC 68071-5006 Acyclovir
Product NDC 68071-5006
11-digit product format 680715006
Labeler code 68071
Product ID 68071-5006_bbb3355a-44a4-a3f4-e053-2a95a90a0e6e
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 400 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 68071-5006-3 68071500603 30 TABLET in 1 BOTTLE (68071-5006-3) 30 tablet 2019-07-29 0000-00-00 No No Current