Acyclovir

Product NDC: 69097-656
11-digit product format: 690970656
Labeler code: 69097
Product ID: 69097-656_38490f0b-817a-4f99-ada0-06d8854b5c75
Type: HUMAN PRESCRIPTION DRUG
Nonproprietary name: Acyclovir
Dosage form: OINTMENT
Route: TOPICAL
Labeler: Cipla USA Inc.
Application: ANDA211794
Marketing category: ANDA
Marketing start: 2019-01-18
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

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
69097-656	ACYCLOVIR OINTMENT [CIPLA USA INC.]	2	Legacy NDC	20210316_ec6b2ffd-8efe-4f5d-8f01-52f1011fccce.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
69097-656-38	69097065638	1 TUBE in 1 CARTON (69097-656-38) > 15 g in 1 TUBE	1 tube	2019-01-18	0000-00-00	No	No	Current
69097-656-40	69097065640	1 TUBE in 1 CARTON (69097-656-40) > 30 g in 1 TUBE	1 tube	2019-01-18	0000-00-00	No	No	Current