tizanidine

Product NDC: 63629-6432
11-digit product format: 636296432
Labeler code: 63629
Product ID: 63629-6432_df79802c-8d51-4541-862e-db4a55bdc0d3
Type: HUMAN PRESCRIPTION DRUG
Nonproprietary name: tizanidine
Dosage form: TABLET
Route: ORAL
Labeler: Bryant Ranch Prepack
Application: ANDA076533
Marketing category: ANDA
Marketing start: 2004-01-16
Marketing end: 0000-00-00
Substance: TIZANIDINE HYDROCHLORIDE
Active strength: 4 mg/1
Pharmacologic classes: Adrenergic alpha2-Agonists [MoA],Central alpha-2 Adrenergic Agonist [EPC]
NDC exclude flag: No
Listing certified through: 2021-12-31
Current FDA listing: Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
63629-6432-1	2020-10-16	C162847	48780-1	9d75b9d0-ae01-f424-e053-dadaa90a57ce	61504053-e4b3-436c-beea-4d6b15ebd8b9
63629-6432-1	2020-01-31	C162847	48780-1	9d75b9d0-ae01-f424-e053-dadaa90a57ce	61504053-e4b3-436c-beea-4d6b15ebd8b9

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
B53E3NMY5C	TIZANIDINE HYDROCHLORIDE	64461-82-1	TIZANIDINE HYDROCHLORIDE
6AI06C00GW	TIZANIDINE	51322-75-9	tizanidine

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
63629-6432-1	63629643201	90 TABLET in 1 BOTTLE (63629-6432-1)	90 tablet	2015-09-17	0000-00-00	No	No	Current