Acyclovir

Product NDC: 51079-550
11-digit product format: 510790550
Labeler code: 51079
Product ID: 51079-550_d4eb8a9f-0218-a52d-e053-2995a90a97af
Type: HUMAN PRESCRIPTION DRUG
Nonproprietary name: acyclovir
Dosage form: OINTMENT
Route: TOPICAL
Labeler: Mylan Institutional Inc.
Application: ANDA202459
Marketing category: ANDA
Marketing start: 2013-11-27
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: 2023-12-31
Current FDA listing: Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
51079-550-67	GM - Gram	51079-550	df76b7dd-84ea-4d31-bd26-4225f29086f5	1	2014-01-04
51079-550-68	GM - Gram	51079-550	9e1e5b4a-8b74-4c58-9322-b76813f82038	1	2014-01-04

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
51079-550-68	51079055068	2 TUBE in 1 CARTON (51079-550-68) > 5 g in 1 TUBE (51079-550-67)	2 tube	2013-11-27	0000-00-00	No	No	Current