acyclovir

Product NDC
72789-536
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
acyclovir
Dosage form
CAPSULE
Route
ORAL
Labeler
PD-Rx Pharmaceuticals, Inc.
Application
ANDA204313
Marketing category
ANDA
Substance
ACYCLOVIR
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
72789-536-5050 CAPSULE in 1 BOTTLE, PLASTIC (72789-536-50) 2025-12-02NoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Acyclovir Capsules, USP Rx onlyPD-Rx Pharmaceuticals, Inc.2025-12-03HUMAN PRESCRIPTION DRUG LABEL1