Acyclovir

Product NDC
72162-1908
11-digit product format
721621908
Labeler code
72162
Product ID
72162-1908_b14c9945-fd73-48e0-af82-302ccf0184ff
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Acyclovir
Dosage form
CAPSULE
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
ANDA075090
Marketing category
ANDA
Marketing start
2021-05-27
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
2026-12-31
Current FDA listing
Yes

Related Records

Related UNII Ingredients

UNIIPreferred termRegistry numberMatched term
X4HES1O11FACYCLOVIR59277-89-3ACYCLOVIR

Packages

Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
72162-1908-07216219080030 CAPSULE in 1 BOTTLE (72162-1908-0) 30 capsule2023-05-08NoNoHistorical
72162-1908-17216219080125 CAPSULE in 1 BOTTLE (72162-1908-1) 25 capsule2023-05-08NoNoHistorical
72162-1908-27216219080235 CAPSULE in 1 BOTTLE (72162-1908-2) 35 capsule2023-05-08NoNoHistorical
72162-1908-37216219080350 CAPSULE in 1 BOTTLE (72162-1908-3) 50 capsule2023-05-08NoNoHistorical
72162-1908-472162190804100 CAPSULE in 1 BOTTLE (72162-1908-4) 100 capsule2023-05-08NoNoHistorical
72162-1908-57216219080540 CAPSULE in 1 BOTTLE (72162-1908-5) 40 capsule2023-05-08NoNoHistorical
72162-1908-67216219080660 CAPSULE in 1 BOTTLE (72162-1908-6) 60 capsule2023-05-08NoNoHistorical
72162-1908-772162190807120 CAPSULE in 1 BOTTLE (72162-1908-7) 120 capsule2023-05-08NoNoHistorical
72162-1908-87216219080820 CAPSULE in 1 BOTTLE (72162-1908-8) 20 capsule2023-05-08NoNoHistorical
72162-1908-97216219080990 CAPSULE in 1 BOTTLE (72162-1908-9) 90 capsule2023-05-08NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Acyclovir Capsules USPBryant Ranch Prepack2023-05-08HUMAN PRESCRIPTION DRUG LABEL100