Home NDC 55700-539 Acyclovir
Product NDC 55700-539
11-digit product format 557000539
Labeler code 55700
Product ID 55700-539_3dd8341e-0d3b-42d6-af9c-5c97e76c6185
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name Acyclovir
Dosage form TABLET
Route ORAL
Labeler Quality Care Products, LLC
Application ANDA075382
Marketing category ANDA
Marketing start 2009-10-22
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 2023-12-31
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 55700-539-35 55700053935 35 TABLET in 1 BOTTLE, PLASTIC (55700-539-35) 35 tablet 2020-02-07 0000-00-00 No No Current 55700-539-40 55700053940 40 TABLET in 1 BOTTLE, PLASTIC (55700-539-40) 40 tablet 2020-02-11 0000-00-00 No No Current