Albuterol Sulfate
- Product NDC
- 33261-789
- 11-digit product format
- 332610789
- Labeler code
- 33261
- Product ID
- 33261-789_4649abda-b4ec-41f8-b1bc-d1ae0aade616
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Albuterol Sulfate
- Dosage form
- SOLUTION
- Route
- RESPIRATORY (INHALATION)
- Labeler
- Aidarex Pharmaceuticals LLC
- Application
- ANDA077839
- Marketing category
- ANDA
- Marketing start
- 2011-12-05
- Marketing end
- 0000-00-00
- Substance
- ALBUTEROL SULFATE
- Active strength
- 3 mg/3mL
- Pharmacologic classes
- Adrenergic beta2-Agonists [MoA],beta2-Adrenergic Agonist [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 33261-789-01 | Albuterol Sulfate | 1 in 1 CARTON | SOLUTION | 1 | | 1 |
| 33261-789-01 | Albuterol Sulfate | 25 in 1 POUCH | SOLUTION | 25 | | 1 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 33261-789 | ALBUTEROL SULFATE SOLUTION [AIDAREX PHARMACEUTICALS LLC] | 1 | Legacy NDC, 2 package rows | 20131203_05f7916c-52f7-4a4f-a19b-f5e35f02fd0b.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 33261-789-01 | 33261078901 | 1 in 1 CARTON | Historical |