acyclovir

Product NDC: 23155-485
11-digit product format: 231550485
Labeler code: 23155
Product ID: 23155-485_c0594eca-1c4d-41f5-a1ba-194fce06ae30
Type: HUMAN PRESCRIPTION DRUG
Nonproprietary name: acyclovir
Dosage form: SUSPENSION
Route: ORAL
Labeler: Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.
Application: ANDA212718
Marketing category: ANDA
Marketing start: 2020-04-23
Marketing end: 0000-00-00
Substance: ACYCLOVIR
Active strength: 200 mg/5mL
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: 2021-12-31
Current FDA listing: Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
23155-485-51	ML - Milliliter	23155-485	11e07b14-4c11-4a9f-a42c-b19b332746d4	1	2021-07-15

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
X4HES1O11F	ACYCLOVIR	59277-89-3	ACYCLOVIR

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
23155-485-51	23155048551	473 mL in 1 BOTTLE (23155-485-51)	473 ml	2020-04-23	0000-00-00	No	No	Current