Tabradol

Product NDC: 43093-101
11-digit product format: 430930101
Labeler code: 43093
Product ID: 43093-101_28c7b9e3-07ca-6f9b-e054-00144ff88e88
Type: HUMAN PRESCRIPTION DRUG
Nonproprietary name: Cyclobenzaprine Hydrochloride
Dosage form: KIT
Route: ORAL
Labeler: Fusion Pharmaceuticals LLC
Marketing category: UNAPPROVED DRUG OTHER
Marketing start: 2009-09-17
Marketing end: 0000-00-00
Active strength: 0
NDC exclude flag: E
Listing certified through: 2018-12-31
Current FDA listing: Historical FDA.report record

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
51048710-225c-aa41-d0e7-eed095d02838	Product name	4	20250331
d5e51f11-ad28-caa4-4b49-4143974782ad	Product name	1	20150831
c2c26dc9-7e16-fc02-7eba-6b46ed3515ee	Product name	1	20140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
43093-101-01	2020-01-31	C162847	48780-1	9d75b9d0-544c-f424-e053-dadaa90a57ce	TABRADOL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
43093-101-01	Tabradol	1 in 1 KIT	KIT	1		9

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
43093-101-01	ML - Milliliter	43093-101	b835bb30-950b-4a7a-9a85-3c48caecfd2e	1	2015-10-02

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
43093-101	TABRADOL (CYCLOBENZAPRINE HYDROCHLORIDE) KIT [FUSION PHARMACEUTICALS LLC]	9	Legacy NDC, 1 package rows	20160108_5d19ef8b-eef3-4d52-95f5-929765ca6dc7.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Status
43093-101-01	43093010101	1 in 1 KIT	Historical