acyclovir

Product NDC: 51655-099
11-digit product format: 516550099
Labeler code: 51655
Product ID: 51655-099_b4cd2005-abc9-46fd-9209-df6b57b8f730
Type: HUMAN PRESCRIPTION DRUG
Nonproprietary name: Acyclovir
Dosage form: TABLET
Route: ORAL
Labeler: Northwind Pharmaceuticals
Application: ANDA075382
Marketing category: ANDA
Marketing start: 2014-05-14
Marketing end: 0000-00-00
Substance: ACYCLOVIR
Active strength: 800 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: E
Listing certified through: 2018-12-31
Current FDA listing: Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
51655-099-51	2026-01-13	C162847	48780-1	9d75b9cf-ef84-f424-e053-dadaa90a57ce	49bacf64-4707-4ffe-90fa-0cf883aa065f
51655-099-51	2020-01-31	C162847	48780-1	9d75b9cf-ef84-f424-e053-dadaa90a57ce	49bacf64-4707-4ffe-90fa-0cf883aa065f

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

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
51655-099	ACYCLOVIR TABLET [NORTHWIND PHARMACEUTICALS]	1	Legacy NDC	20140617_49bacf64-4707-4ffe-90fa-0cf883aa065f.zip