acyclovir

Product NDC: 68071-2488
11-digit product format: 680712488
Labeler code: 68071
Product ID: 68071-2488_c8be6955-2640-0e9a-e053-2995a90a9a27
Type: HUMAN PRESCRIPTION DRUG
Nonproprietary name: acyclovir
Dosage form: OINTMENT
Route: TOPICAL
Labeler: NuCare Pharmaceuticals,Inc.
Application: ANDA205974
Marketing category: ANDA
Marketing start: 2020-06-08
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
68071-2488-3	2023-01-30	C162847	48780-1	f386c649-dcfc-0266-e053-dadaa90a7c1a	c8be6955-263f-0e9a-e053-2995a90a9a27

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
68071-2488	ACYCLOVIR OINTMENT [NUCARE PHARMACEUTICALS,INC.]	1	Legacy NDC	20210805_c8be6955-263f-0e9a-e053-2995a90a9a27.zip

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
68071-2488-3	68071248803	1 TUBE in 1 CARTON (68071-2488-3) > 30 g in 1 TUBE	1 tube	2021-08-04	0000-00-00	No	No	Current