Acyclovir

Product NDC: 68071-5157
11-digit product format: 680715157
Labeler code: 68071
Product ID: 68071-5157_bbf60b5c-ebdd-6c46-e053-2995a90a7365
Type: HUMAN PRESCRIPTION DRUG
Nonproprietary name: Acyclovir
Dosage form: OINTMENT
Route: TOPICAL
Labeler: NuCare Pharmaceuticals,Inc.
Application: ANDA206437
Marketing category: ANDA
Marketing start: 2017-08-18
Marketing end: 0000-00-00
Substance: ACYCLOVIR
Active strength: 50 mg/g
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
68071-5157-3	2024-06-20	C162847	48780-1	f386c64a-1e8b-0266-e053-dadaa90a7c1a	9cc1d1ae-e265-2ccb-e053-2a95a90ae8ea
68071-5157-3	2023-01-30	C162847	48780-1	f386c64a-1e8b-0266-e053-dadaa90a7c1a	9cc1d1ae-e265-2ccb-e053-2a95a90ae8ea

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
68071-5157-3	68071515703	30 g in 1 BOX (68071-5157-3)	30 g	2020-01-22	0000-00-00	No	No	Current