Acyclovir

Product NDC: 55700-651
11-digit product format: 557000651
Labeler code: 55700
Product ID: 55700-651_ec9af19c-779c-4d4b-87e9-3308d7a8eb05
Type: HUMAN PRESCRIPTION DRUG
Nonproprietary name: Acyclovir
Dosage form: CAPSULE
Route: ORAL
Labeler: Lake Erie Medical DBA Quality Care Products LLC
Application: ANDA075090
Marketing category: ANDA
Marketing start: 2018-07-06
Marketing end: 0000-00-00
Substance: ACYCLOVIR
Active strength: 200 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: 2020-12-31
Current FDA listing: Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
55700-651-30	2024-11-20	C162847	48780-1	f386c649-9d64-0266-e053-dadaa90a7c1a	23bd6eed-263f-467e-aafb-e6c5161b98e8
55700-651-30	2023-01-30	C162847	48780-1	f386c649-9d64-0266-e053-dadaa90a7c1a	23bd6eed-263f-467e-aafb-e6c5161b98e8

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
55700-651-30	55700065130	30 CAPSULE in 1 BOTTLE (55700-651-30)	30 capsule	2018-07-06	0000-00-00	No	No	Current