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NASACORT AQ
NASACORT AQ - 0075-1506-16 - (triamcinolone acetonide)
Drug Information of NASACORT AQ
| Product NDC: | 0075-1506 |
| Proprietary Name: | NASACORT AQ |
| Non Proprietary Name: | triamcinolone acetonide |
| Active Ingredient(s): | 55 ug/1 & nbsp; triamcinolone acetonide |
| Administration Route(s): | NASAL |
| Dosage Form(s): | SPRAY, METERED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of NASACORT AQ
| Product NDC: | 0075-1506 |
| Labeler Name: | sanofi-aventis U.S. LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA020468 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19960520 |
Package Information of NASACORT AQ
| Package NDC: | 0075-1506-16 |
| Package Description: | 120 SPRAY, METERED in 1 BOTTLE, SPRAY (0075-1506-16) |
NDC Information of NASACORT AQ
| NDC Code | 0075-1506-16 |
| Proprietary Name | NASACORT AQ |
| Package Description | 120 SPRAY, METERED in 1 BOTTLE, SPRAY (0075-1506-16) |
| Product NDC | 0075-1506 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | triamcinolone acetonide |
| Dosage Form Name | SPRAY, METERED |
| Route Name | NASAL |
| Start Marketing Date | 19960520 |
| Marketing Category Name | NDA |
| Labeler Name | sanofi-aventis U.S. LLC |
| Substance Name | TRIAMCINOLONE ACETONIDE |
| Strength Number | 55 |
| Strength Unit | ug/1 |
| Pharmaceutical Classes |
