Home NDC 68788-7436 Acyclovir
Product NDC 68788-7436
11-digit product format 687887436
Labeler code 68788
Product ID 68788-7436_b896a576-9d98-4e11-9da1-9d81199e7c1f
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name Acyclovir
Dosage form TABLET
Route ORAL
Labeler Preferred 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 Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 68788-7436-2 68788743602 21 TABLET in 1 BOTTLE (68788-7436-2) 21 tablet 2019-10-04 0000-00-00 No No Current 68788-7436-3 68788743603 30 TABLET in 1 BOTTLE (68788-7436-3) 30 tablet 2019-10-04 0000-00-00 No No Current 68788-7436-4 68788743604 40 TABLET in 1 BOTTLE (68788-7436-4) 40 tablet 2019-10-04 0000-00-00 No No Current 68788-7436-5 68788743605 50 TABLET in 1 BOTTLE (68788-7436-5) 50 tablet 2019-10-04 0000-00-00 No No Current 68788-7436-6 68788743606 60 TABLET in 1 BOTTLE (68788-7436-6) 60 tablet 2019-10-04 0000-00-00 No No Current 68788-7436-7 68788743607 25 TABLET in 1 BOTTLE (68788-7436-7) 25 tablet 2019-10-04 0000-00-00 No No Current 68788-7436-8 68788743608 35 TABLET in 1 BOTTLE (68788-7436-8) 35 tablet 2019-10-04 0000-00-00 No No Current