Acyclovir

Product NDC
71205-578
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Acyclovir
Dosage form
CAPSULE
Route
ORAL
Labeler
Proficient Rx LP
Application
ANDA206261
Marketing category
ANDA
Substance
ACYCLOVIR
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
71205-578-3030 CAPSULE in 1 BOTTLE, PLASTIC (71205-578-30) 2021-06-10NoHistorical
71205-578-6060 CAPSULE in 1 BOTTLE, PLASTIC (71205-578-60) 2021-06-10NoHistorical
71205-578-9090 CAPSULE in 1 BOTTLE, PLASTIC (71205-578-90) 2021-06-10NoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
PRESCRIBING INFORMATION Acyclovir Capsules USPProficient Rx LP2022-08-01HUMAN PRESCRIPTION DRUG LABEL2