Acyclovir

Product NDC

0713-0630

11-digit product format

007130630

Labeler code

0713

Product ID

0713-0630_de0c0ab2-9e0b-a0b7-e053-2995a90acdd4

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Acyclovir

Dosage form

OINTMENT

Route

TOPICAL

Labeler

Cosette Pharmaceuticals, Inc.

Application

ANDA205591

Marketing category

ANDA

Marketing start

2017-11-13

Marketing end

2023-10-31

Substance

ACYCLOVIR

Active strength

50 mg/g

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

0000-00-00

Current FDA listing

Historical FDA.report record