Albuterol Sulfate
- Product NDC
- 62135-828
- 11-digit product format
- 621350828
- Labeler code
- 62135
- Product ID
- 62135-828_11e5a7ae-f1eb-ea1f-e063-6294a90a0efb
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Albuterol Sulfate
- Dosage form
- SOLUTION
- Route
- RESPIRATORY (INHALATION)
- Labeler
- Chartwell RX, LLC
- Application
- ANDA074880
- Marketing category
- ANDA
- Marketing start
- 1997-09-17
- 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
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Albuterol Sulfate
- Listing expiration
- 2026-12-31
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 |
|---|
| 62135-828-84 | Albuterol Sulfate | 6 in 1 CARTON | SOLUTION | 6 | | 3 |
| 62135-828-84 | Albuterol Sulfate | 5 in 1 POUCH | SOLUTION | 5 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 62135-828 | ALBUTEROL SULFATE SOLUTION [CHARTWELL RX, LLC] | 3 | Current NDC, 2 package rows | 20240222_922bf33b-4d55-4c35-9f68-72efbb17c14f.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 |
|---|
| 62135-828-84 | 62135082884 | 6 POUCH in 1 CARTON (62135-828-84) / 5 VIAL in 1 POUCH / 3 mL in 1 VIAL | 6 pouch | 2024-01-18 | No | No | Current |