Home NDC 70934-800 Acyclovir
Product NDC 70934-800
11-digit product format 709340800
Labeler code 70934
Product ID 70934-800_da6f0391-dc87-200e-e053-2995a90a0f39
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name Acyclovir
Dosage form CAPSULE
Route ORAL
Labeler Denton Pharma, Inc. DBA Northwind Pharmaceuticals
Application ANDA075090
Marketing category ANDA
Marketing start 2020-10-22
Marketing end 2024-04-30
Substance ACYCLOVIR
Active strength 200 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 0000-00-00
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 70934-800-25 70934080025 25 CAPSULE in 1 BOTTLE, PLASTIC (70934-800-25) 25 capsule 2022-03-14 2023-10-31 No No Current 70934-800-30 70934080030 30 CAPSULE in 1 BOTTLE, PLASTIC (70934-800-30) 30 capsule 2020-10-22 0000-00-00 No No Current