Albuterol Sulfate
- Product NDC
- 55154-2132
- 11-digit product format
- 551542132
- Labeler code
- 55154
- Product ID
- 55154-2132_0b6d1c1d-c2f5-457c-a9aa-0bff7c138fc6
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Albuterol Sulfate
- Dosage form
- SOLUTION
- Route
- RESPIRATORY (INHALATION)
- Labeler
- Cardinal Health 107, LLC
- Application
- ANDA077839
- Marketing category
- ANDA
- Marketing start
- 2023-01-16
- Substance
- ALBUTEROL SULFATE
- Active strength
- 2.5 mg/3mL
- Pharmacologic classes
- Adrenergic beta2-Agonists [MoA], beta2-Adrenergic Agonist [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Albuterol Sulfate
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ALBUTEROL SULFATE | 2.5 mg/3mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 021SEF3731 |
| Rxcui | 630208 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 55154-2132-5 | Albuterol Sulfate | 1 in 1 POUCH | SOLUTION | 1 | | 5 |
| 55154-2132-5 | Albuterol Sulfate | 5 in 1 BAG | SOLUTION | 5 | | 5 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 55154-2132 | ALBUTEROL SULFATE SOLUTION [CARDINAL HEALTH 107, LLC] | 3 | Current NDC, 2 package rows | 20240820_6ec88f64-66a2-4ca9-9913-c192fc33f88b.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 55154-2132-5 | 55154213205 | 5 POUCH in 1 BAG (55154-2132-5) / 1 AMPULE in 1 POUCH / 3 mL in 1 AMPULE | 5 pouch | 2023-01-16 | No | No | Current |