Albuterol Sulfate
- Product NDC
- 68788-8874
- 11-digit product format
- 687888874
- Labeler code
- 68788
- Product ID
- 68788-8874_1c72fd84-7dbc-45d0-ab88-fb4221ce369f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Albuterol Sulfate
- Dosage form
- INHALANT
- Route
- RESPIRATORY (INHALATION)
- Labeler
- Preferred Pharmaceuticals Inc.
- Application
- ANDA209959
- Marketing category
- ANDA
- Marketing start
- 2025-05-16
- Substance
- ALBUTEROL SULFATE
- Active strength
- 90 ug/1
- 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 | 90 ug/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 021SEF3731 |
| Rxcui | 2123111 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 68788-8874-2 | Albuterol Sulfate | 200 in 1 CANISTER | INHALANT | 200 | | 1 |
| 68788-8874-2 | Albuterol Sulfate | 1 in 1 CARTON | INHALANT | 1 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 68788-8874 | ALBUTEROL SULFATE INHALANT [PREFERRED PHARMACEUTICALS INC.] | 1 | Current NDC, 2 package rows | 20250521_1c72fd84-7dbc-45d0-ab88-fb4221ce369f.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 |
|---|
| 68788-8874-2 | 68788887402 | 1 CANISTER in 1 CARTON (68788-8874-2) / 200 INHALANT in 1 CANISTER | 1 canister | 2025-05-16 | No | No | Current |