PULMICORT
- Product NDC
- 50090-7867
- 11-digit product format
- 500907867
- Labeler code
- 50090
- Product ID
- 50090-7867_c80d7c71-8f2c-430e-a6ca-3b4dbc57451f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Budesonide
- Dosage form
- AEROSOL, POWDER
- Route
- RESPIRATORY (INHALATION)
- Labeler
- A-S Medication Solutions
- Application
- NDA021949
- Marketing category
- NDA
- Marketing start
- 2025-07-01
- Substance
- BUDESONIDE
- Active strength
- 180 ug/1
- Pharmacologic classes
- Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- PULMICORT
- Brand name suffix
- FLEXHALER
- Listing expiration
- 2027-12-31
Active Ingredients#
| Ingredient | Strength |
|---|---|
| BUDESONIDE | 180 ug/1 |
Harmonized Identifiers#
| Field | Values |
|---|---|
| Unii | Q3OKS62Q6X |
| Rxcui | 966522, 966524 |
DailyMed Product Concepts#
| Product concept | Relation | Version | Effective |
|---|---|---|---|
| 7816cdf6-b925-4282-bedd-11ae25d518a1 | Product name | 1 | 20250116 |
| d17a61d0-e77b-4bcb-ad22-343ff1a3ef4d | Product name | 2 | 20240424 |
| 9ab9f611-cedd-47ea-a83c-0489c8c04fc6 | Product name | 1 | 20231006 |
| c76bcd0f-25eb-471e-b970-1956c95c26c5 | Product name | 1 | 20230425 |
| a03aea00-1d8b-bfad-a82e-f52f68676f63 | Product name | 2 | 20221216 |
| 54a29484-7dde-4771-9547-005149321621 | Product name | 1 | 20220720 |
| 793b53dd-c0ea-da17-9ac0-fb5c4a6e0743 | Product name | 5 | 20211018 |
| 218c043e-94e5-4e66-a363-d0d446485bc6 | Product name | 2 | 20210512 |
| 7d8c8d5a-f174-4e6b-97b1-6fd615c5df9a | Product name | 1 | 20210204 |
| 5e2e25b6-cb6b-8e81-afe3-62c3e2cd56c7 | Product name | 9 | 20210127 |
| da63bc8c-2e89-4044-89d6-1facbff5474e | Product name | 1 | 20200121 |
| 899766bc-33ce-8154-910d-12cb0889fb56 | Product name | 2 | 20150106 |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 50090-7867-0 | PULMICORTFLEXHALER | 1 in 1 CARTON | AEROSOL, POWDER | 1 | 2 | |
| 50090-7867-0 | PULMICORTFLEXHALER | 120 in 1 INHALER | AEROSOL, POWDER | 120 | 2 |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 50090-7867-0 | EA - Each | 50090-7867 | 8af323ba-bb18-4f02-bb12-d6ea8c4cf93e | 1 | 2026-03-17 |
DailyMed RxNorm Mappings#
| RxCUI | RxNorm string | TTY | DailyMed | SPL version |
|---|---|---|---|---|
| 966522 | budesonide 180 MCG/INHAL Dry Powder Inhaler, 120 ACTUAT | PSN | 5d0c6c7e-2f53-4238-ab34-bd8cf49d8a66 | 2 |
| 966524 | Pulmicort Flexhaler 180 MCG/INHAL Dry Powder Inhaler, 120 ACTUAT | PSN | 5d0c6c7e-2f53-4238-ab34-bd8cf49d8a66 | 2 |
| 966524 | 120 ACTUAT budesonide 0.18 MG/ACTUAT Dry Powder Inhaler [Pulmicort] | SBD | 5d0c6c7e-2f53-4238-ab34-bd8cf49d8a66 | 2 |
| 966522 | 120 ACTUAT budesonide 0.18 MG/ACTUAT Dry Powder Inhaler | SCD | 5d0c6c7e-2f53-4238-ab34-bd8cf49d8a66 | 2 |
| 966522 | budesonide 0.18 MG/ACTUAT (0.16 MG/ACTUAT from the mouthpiece) Dry Powder Inhaler, 120 ACTUAT | SY | 5d0c6c7e-2f53-4238-ab34-bd8cf49d8a66 | 2 |
| 966522 | budesonide 180 MCG/ACTUAT Dry Powder Inhaler, 120 ACTUATS | SY | 5d0c6c7e-2f53-4238-ab34-bd8cf49d8a66 | 2 |
| 966524 | Pulmicort Flexhaler 0.18 MG/ACTUAT (0.16 MG/ACTUAT from the mouthpiece) Dry Powder Inhaler, 120 ACTUAT | SY | 5d0c6c7e-2f53-4238-ab34-bd8cf49d8a66 | 2 |
| 966524 | Pulmicort Flexhaler 180 MCG/ACTUAT Dry Powder Inhaler, 120 ACTUAT | SY | 5d0c6c7e-2f53-4238-ab34-bd8cf49d8a66 | 2 |
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|
| 50090-7867-0 | 50090786700 | 1 INHALER in 1 CARTON (50090-7867-0) / 120 AEROSOL, POWDER in 1 INHALER | 1 inhaler | 2026-01-27 | No | No | Current |