ZOLMITRIPTAN

Product NDC: 31722-459
11-digit product format: 317220459
Labeler code: 31722
Product ID: 31722-459_117e0844-95dd-4d5c-88b5-e02a2a3a3125
Type: HUMAN PRESCRIPTION DRUG
Nonproprietary name: ZOLMITRIPTAN
Dosage form: TABLET, FILM COATED
Route: ORAL
Labeler: Camber Pharmaceuticals Inc
Application: ANDA204284
Marketing category: ANDA
Marketing start: 2015-01-05
Marketing end: 0000-00-00
Substance: ZOLMITRIPTAN
Active strength: 5 mg/1
Pharmacologic classes: Serotonin 1b Receptor Agonists [MoA],Serotonin 1d Receptor Agonists [MoA],Serotonin-1b and Serotonin-1d Receptor Agonist [EPC]
NDC exclude flag: E
Listing certified through: 2017-12-31
Current FDA listing: Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
31722-459-03	2025-06-18	C162847	48780-1	9d75b9cf-d670-f424-e053-dadaa90a57ce	ac89615d-7618-4c7c-8d4e-1bc74b1f7141
31722-459-03	2020-01-31	C162847	48780-1	9d75b9cf-d670-f424-e053-dadaa90a57ce	ac89615d-7618-4c7c-8d4e-1bc74b1f7141

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
31722-459	ZOLMITRIPTAN TABLET, FILM COATED [CAMBER PHARMACEUTICALS INC]	2	Legacy NDC	20150121_ac89615d-7618-4c7c-8d4e-1bc74b1f7141.zip