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BECONASE
BECONASE - 0173-0388-79 - (beclomethasone dipropionate monohydrate)
Drug Information of BECONASE
| Product NDC: | 0173-0388 |
| Proprietary Name: | BECONASE |
| Non Proprietary Name: | beclomethasone dipropionate monohydrate |
| Active Ingredient(s): | 42 ug/1 & nbsp; beclomethasone dipropionate monohydrate |
| Administration Route(s): | NASAL |
| Dosage Form(s): | SPRAY, SUSPENSION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of BECONASE
| Product NDC: | 0173-0388 |
| Labeler Name: | GlaxoSmithKline LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA019389 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19891001 |
Package Information of BECONASE
| Package NDC: | 0173-0388-79 |
| Package Description: | 180 SPRAY, SUSPENSION in 1 BOTTLE, PUMP (0173-0388-79) |
NDC Information of BECONASE
| NDC Code | 0173-0388-79 |
| Proprietary Name | BECONASE |
| Package Description | 180 SPRAY, SUSPENSION in 1 BOTTLE, PUMP (0173-0388-79) |
| Product NDC | 0173-0388 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | beclomethasone dipropionate monohydrate |
| Dosage Form Name | SPRAY, SUSPENSION |
| Route Name | NASAL |
| Start Marketing Date | 19891001 |
| Marketing Category Name | NDA |
| Labeler Name | GlaxoSmithKline LLC |
| Substance Name | BECLOMETHASONE DIPROPIONATE MONOHYDRATE |
| Strength Number | 42 |
| Strength Unit | ug/1 |
| Pharmaceutical Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |
