RHINOCORT Allergy is a Nasal Spray, Metered in the Human Otc Drug category. It is labeled and distributed by Johnson & Johnson Consumer Inc., Mcneil Consumer Healthcare Division. The primary component is Budesonide.
Product ID | 50580-646_2100d000-ef0a-494f-a0af-b572d9eb99b1 |
NDC | 50580-646 |
Product Type | Human Otc Drug |
Proprietary Name | RHINOCORT Allergy |
Generic Name | Budesonide |
Dosage Form | Spray, Metered |
Route of Administration | NASAL |
Marketing Start Date | 2016-01-14 |
Marketing Category | NDA / NDA |
Application Number | NDA020746 |
Labeler Name | Johnson & Johnson Consumer Inc., McNeil Consumer Healthcare Division |
Substance Name | BUDESONIDE |
Active Ingredient Strength | 32 ug/1 |
NDC Exclude Flag | N |
Listing Certified Through | 2021-12-31 |
Marketing Start Date | 2016-01-14 |
NDC Exclude Flag | N |
Sample Package? | N |
Marketing Category | NDA |
Application Number | NDA020746 |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2016-01-14 |
Marketing Category | NDA |
Application Number | NDA020746 |
Product Type | HUMAN OTC DRUG |
Billing Unit | ML |
Marketing Start Date | 2016-01-14 |
Marketing Category | NDA |
Application Number | NDA020746 |
Product Type | HUMAN OTC DRUG |
Billing Unit | ML |
Marketing Start Date | 2016-01-14 |
Ingredient | Strength |
---|---|
BUDESONIDE | 32 ug/1 |
SPL SET ID: | 1ae1c5e8-16c6-4799-9a62-96d974c30f1f |
Manufacturer | |
UNII | |
RxNorm Concept Unique ID - RxCUI | |
UPC Code |
NDC | Brand Name | Generic Name |
---|---|---|
50580-646 | RHINOCORT Allergy | RHINOCORT Allergy |
0093-6815 | Budesonide | Budesonide |
0093-6816 | Budesonide | Budesonide |
0093-6817 | Budesonide | Budesonide |
0093-7445 | Budesonide | Budesonide |
0115-1687 | Budesonide Inhalation | Budesonide |
0115-1689 | Budesonide Inhalation | Budesonide |
0186-0916 | PULMICORT | Budesonide |
0186-0917 | PULMICORT | Budesonide |
0186-1988 | PULMICORT RESPULES | Budesonide |
0186-1989 | PULMICORT RESPULES | Budesonide |
0186-1990 | PULMICORT RESPULES | Budesonide |