ZOMIG ZMT - 0310-0213-21 - (Zolmitriptan)

Alphabetical Index


Drug Information of ZOMIG ZMT

Product NDC: 0310-0213
Proprietary Name: ZOMIG ZMT
Non Proprietary Name: Zolmitriptan
Active Ingredient(s): 5    mg/1 & nbsp;   Zolmitriptan
Administration Route(s): ORAL
Dosage Form(s): TABLET, ORALLY DISINTEGRATING
Coding System: National Drug Codes(NDC)

Labeler Information of ZOMIG ZMT

Product NDC: 0310-0213
Labeler Name: AstraZeneca Pharmaceuticals LP
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021231
Marketing Category: NDA
Start Marketing Date: 20011001

Package Information of ZOMIG ZMT

Package NDC: 0310-0213-21
Package Description: 3 BLISTER PACK in 1 CARTON (0310-0213-21) > 3 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK

NDC Information of ZOMIG ZMT

NDC Code 0310-0213-21
Proprietary Name ZOMIG ZMT
Package Description 3 BLISTER PACK in 1 CARTON (0310-0213-21) > 3 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK
Product NDC 0310-0213
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Zolmitriptan
Dosage Form Name TABLET, ORALLY DISINTEGRATING
Route Name ORAL
Start Marketing Date 20011001
Marketing Category Name NDA
Labeler Name AstraZeneca Pharmaceuticals LP
Substance Name ZOLMITRIPTAN
Strength Number 5
Strength Unit mg/1
Pharmaceutical Classes Serotonin 1b Receptor Agonists [MoA],Serotonin 1d Receptor Agonists [MoA],Serotonin-1b and Serotonin-1d Receptor Agonist [EPC]

Complete Information of ZOMIG ZMT


General Information