Acyclovir

Product NDC: 55700-786
11-digit product format: 557000786
Labeler code: 55700
Product ID: 55700-786_cc7194ad-4de6-44b8-86fe-62cdbc5ed11f
Type: HUMAN PRESCRIPTION DRUG
Nonproprietary name: Acyclovir
Dosage form: TABLET
Route: ORAL
Labeler: Quality Care Products, LLC
Application: ANDA203834
Marketing category: ANDA
Marketing start: 2019-08-30
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: No
Listing certified through: 2022-12-31
Current FDA listing: Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
55700-786-35	2024-11-20	C162847	48780-1	f386c64a-4988-0266-e053-dadaa90a7c1a	04e24e1f-ac6b-46b9-9ee2-61fb74a4e5ba
55700-786-35	2023-01-30	C162847	48780-1	f386c64a-4988-0266-e053-dadaa90a7c1a	04e24e1f-ac6b-46b9-9ee2-61fb74a4e5ba

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
55700-786-35	55700078635	35 TABLET in 1 BOTTLE (55700-786-35)	35 tablet	2019-08-30	0000-00-00	No	No	Current