Acyclovir

Product NDC: 70518-1942
11-digit product format: 705181942
Labeler code: 70518
Product ID: 70518-1942_c560b9c0-dabe-21aa-e053-2995a90abe44
Type: HUMAN PRESCRIPTION DRUG
Nonproprietary name: Acyclovir
Dosage form: TABLET
Route: ORAL
Labeler: REMEDYREPACK INC.
Application: ANDA210401
Marketing category: ANDA
Marketing start: 2019-03-07
Marketing end: 0000-00-00
Substance: ACYCLOVIR
Active strength: 400 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: 2022-12-31
Current FDA listing: Historical FDA.report record

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
X4HES1O11F	ACYCLOVIR	59277-89-3	ACYCLOVIR

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
70518-1942-0	70518194200	30 TABLET in 1 BLISTER PACK (70518-1942-0)	30 tablet	2019-03-07	0000-00-00	No	No	Current
70518-1942-1	70518194201	30 TABLET in 1 BOTTLE, PLASTIC (70518-1942-1)	30 tablet	2019-08-16	0000-00-00	No	No	Current
70518-1942-2	70518194202	21 TABLET in 1 BOTTLE, PLASTIC (70518-1942-2)	21 tablet	2019-10-04	0000-00-00	No	No	Current