ACYCLOVIR

Product NDC: 51655-678
11-digit product format: 516550678
Labeler code: 51655
Product ID: 51655-678_4509e08a-61f5-4725-9aae-e05104f510ed
Type: HUMAN PRESCRIPTION DRUG
Nonproprietary name: ACYCLOVIR
Dosage form: TABLET
Route: ORAL
Labeler: Northwind Pharmaceuticals
Application: ANDA075382
Marketing category: ANDA
Marketing start: 2015-03-03
Marketing end: 0000-00-00
Substance: ACYCLOVIR
Active strength: 400 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: 2019-12-31
Current FDA listing: Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
51655-678-23	2026-01-08	C162847	48780-1	9d75b9cf-ecba-f424-e053-dadaa90a57ce	e2e6e150-cd11-40b6-8279-de34e8997b90
51655-678-51	2026-01-08	C162847	48780-1	9d75b9cf-ecba-f424-e053-dadaa90a57ce	e2e6e150-cd11-40b6-8279-de34e8997b90
51655-678-23	2020-01-31	C162847	48780-1	9d75b9cf-ecba-f424-e053-dadaa90a57ce	e2e6e150-cd11-40b6-8279-de34e8997b90
51655-678-51	2020-01-31	C162847	48780-1	9d75b9cf-ecba-f424-e053-dadaa90a57ce	e2e6e150-cd11-40b6-8279-de34e8997b90

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version	Uploaded
ACYCLOVIR	ACTIVE INGREDIENT	X4HES1O11F	ACYCLOVIR TABLET [NORTHWIND PHARMACEUTICALS, LLC]	1
ACYCLOVIR	ACTIVE MOIETY	X4HES1O11F	ACYCLOVIR TABLET [NORTHWIND PHARMACEUTICALS, LLC]	1

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
51655-678	ACYCLOVIR TABLET [NORTHWIND PHARMACEUTICALS]	2	Legacy NDC	20170103_e2e6e150-cd11-40b6-8279-de34e8997b90.zip