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NARATRIPTAN HYDROCHLORIDE
NARATRIPTAN HYDROCHLORIDE - 62756-437-69 - (NARATRIPTAN HYDROCHLORIDE)
Drug Information of NARATRIPTAN HYDROCHLORIDE
| Product NDC: | 62756-437 |
| Proprietary Name: | NARATRIPTAN HYDROCHLORIDE |
| Non Proprietary Name: | NARATRIPTAN HYDROCHLORIDE |
| Active Ingredient(s): | 2.5 mg/1 & nbsp; NARATRIPTAN HYDROCHLORIDE |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of NARATRIPTAN HYDROCHLORIDE
| Product NDC: | 62756-437 |
| Labeler Name: | Sun Pharmaceutical Industries Limited |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA091552 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20110222 |
Package Information of NARATRIPTAN HYDROCHLORIDE
| Package NDC: | 62756-437-69 |
| Package Description: | 1 BLISTER PACK in 1 CARTON (62756-437-69) > 9 TABLET, FILM COATED in 1 BLISTER PACK |
NDC Information of NARATRIPTAN HYDROCHLORIDE
| NDC Code | 62756-437-69 |
| Proprietary Name | NARATRIPTAN HYDROCHLORIDE |
| Package Description | 1 BLISTER PACK in 1 CARTON (62756-437-69) > 9 TABLET, FILM COATED in 1 BLISTER PACK |
| Product NDC | 62756-437 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | NARATRIPTAN HYDROCHLORIDE |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20110222 |
| Marketing Category Name | ANDA |
| Labeler Name | Sun Pharmaceutical Industries Limited |
| Substance Name | NARATRIPTAN HYDROCHLORIDE |
| Strength Number | 2.5 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Serotonin 1b Receptor Agonists [MoA],Serotonin 1d Receptor Agonists [MoA],Serotonin-1b and Serotonin-1d Receptor Agonist [EPC] |
