Acyclovir

Product NDC
0093-8943
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Acyclovir
Dosage form
TABLET
Route
ORAL
Labeler
Teva Pharmaceuticals USA, Inc.
Application
ANDA074556
Marketing category
ANDA
Substance
ACYCLOVIR
Current FDA listing
Historical FDA.report record

Related Records

Packages

No records found.

Related DailyMed Labels

Set IDTitleManufacturerEffective dateTypeVersion
4e403fe2-731d-3453-e054-00144ff88e88RedPharm Drug, Inc.2020-01-20HUMAN PRESCRIPTION DRUG LABEL2
34f57b50-d013-2c77-e054-00144ff88e88ACYCLOVIR CAPSULES USP ACYCLOVIR TABLETS USP Rx onlyApotheca Inc.2016-06-10HUMAN PRESCRIPTION DRUG LABEL2
5311b9b2-e4a3-45e3-ac90-64f03740b8ecACYCLOVIR CAPSULES USP ACYCLOVIR TABLETS USP Rx onlyState of Florida DOH Central Pharmacy2014-02-28HUMAN PRESCRIPTION DRUG LABEL1
7b7f90ab-8336-48a2-9762-c23a02f9172eACYCLOVIR CAPSULES USP ACYCLOVIR TABLETS USP 8940 8943 8947 Rx onlyMedVantx, Inc. | Teva Pharmaceuticals USA Inc | Blenheim Pharmacal, Inc.2013-02-08HUMAN PRESCRIPTION DRUG LABEL1
68227df2-cac6-4799-8dcd-8c2f42204315ACYCLOVIR CAPSULES USP ACYCLOVIR TABLETS USP 8940 8943 8947 Rx onlyAidarex Pharmaceuticals LLC2012-09-10HUMAN PRESCRIPTION DRUG LABEL3
c48d04a4-e8ca-4948-a2ff-b45ea44b49b0ACYCLOVIR CAPSULES USP ACYCLOVIR TABLETS USP 8940 8943 8947 Rx onlyBlenheim Pharmacal, Inc.2011-04-29HUMAN PRESCRIPTION DRUG LABEL2