Acyclovir

Product NDC

68071-2235

11-digit product format

680712235

Labeler code

68071

Product ID

68071-2235_d607703e-6f51-e9b0-e053-2a95a90a480a

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Acyclovir

Dosage form

CAPSULE

Route

ORAL

Labeler

NuCare Pharmaceuticals,Inc.

Application

ANDA201445

Marketing category

ANDA

Marketing start

2016-10-15

Marketing end

0000-00-00

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

2023-12-31

Current FDA listing

Historical FDA.report record