Details for New Drug Application (NDA): 020468
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The generic ingredient in NASACORT ALLERGY 24 HOUR is triamcinolone acetonide. There is one drug master file entry for this compound. Eighty suppliers are listed for this compound. Additional details are available on the triamcinolone acetonide profile page.
Summary for 020468
| Tradename: | NASACORT ALLERGY 24 HOUR |
| Applicant: | Chattem Sanofi |
| Ingredient: | triamcinolone acetonide |
| Patents: | 0 |
Pharmacology for NDA: 020468
| Mechanism of Action | Corticosteroid Hormone Receptor Agonists |
Medical Subject Heading (MeSH) Categories for 020468
Suppliers and Packaging for NDA: 020468
| Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
|---|---|---|---|---|---|---|---|---|
| NASACORT ALLERGY 24 HOUR | triamcinolone acetonide | SPRAY, METERED;NASAL | 020468 | NDA | Chattem, Inc. | 41167-5800 | 41167-5800-1 | 1 BOTTLE, SPRAY in 1 CARTON (41167-5800-1) / 30 SPRAY, METERED in 1 BOTTLE, SPRAY |
| NASACORT ALLERGY 24 HOUR | triamcinolone acetonide | SPRAY, METERED;NASAL | 020468 | NDA | Chattem, Inc. | 41167-5800 | 41167-5800-2 | 2 BOTTLE, SPRAY in 1 CARTON (41167-5800-2) / 120 SPRAY, METERED in 1 BOTTLE, SPRAY |
Profile for product number 002
| Active Rx/OTC/Discontinued: | OTC | Dosage: | SPRAY, METERED;NASAL | Strength | 0.055MG/SPRAY | ||||
| Approval Date: | Oct 11, 2013 | TE: | RLD: | Yes | |||||
Expired US Patents for NDA 020468
| Applicant | Tradename | Generic Name | Dosage | NDA | Approval Date | Patent No. | Patent Expiration |
|---|---|---|---|---|---|---|---|
| Chattem Sanofi | NASACORT ALLERGY 24 HOUR | triamcinolone acetonide | SPRAY, METERED;NASAL | 020468-002 | Oct 11, 2013 | 5,976,573 | ⤷ Start Trial |
| Chattem Sanofi | NASACORT ALLERGY 24 HOUR | triamcinolone acetonide | SPRAY, METERED;NASAL | 020468-002 | Oct 11, 2013 | 7,977,045 | ⤷ Start Trial |
| Chattem Sanofi | NASACORT ALLERGY 24 HOUR | triamcinolone acetonide | SPRAY, METERED;NASAL | 020468-002 | Oct 11, 2013 | 6,143,329 | ⤷ Start Trial |
| >Applicant | >Tradename | >Generic Name | >Dosage | >NDA | >Approval Date | >Patent No. | >Patent Expiration |
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