ALBUTEROL SULFATE
- Product NDC
- 76282-679
- 11-digit product format
- 762820679
- Labeler code
- 76282
- Product ID
- 76282-679_3449ab68-28d3-42f5-8d34-329bf6fa0e6b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- albuterol sulfate
- Dosage form
- INHALANT
- Route
- RESPIRATORY (INHALATION)
- Labeler
- Exelan Pharmaceuticals, Inc.
- Application
- ANDA209959
- Marketing category
- ANDA
- Marketing start
- 2021-10-04
- 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 |
|---|
| 76282-679-42 | ALBUTEROL SULFATE | 200 in 1 CANISTER | INHALANT | 200 | | 4 |
| 76282-679-42 | ALBUTEROL SULFATE | 1 in 1 CARTON | INHALANT | 1 | | 4 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 76282-679 | ALBUTEROL SULFATE INHALANT [EXELAN PHARMACEUTICALS, INC.] | 4 | Current NDC, Legacy NDC, 2 package rows | 20220211_29e35e54-dbd6-4426-993f-893d7a4d69be.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 76282-679-42 | 76282067942 | 1 CANISTER in 1 CARTON (76282-679-42) / 200 INHALANT in 1 CANISTER | 1 canister | 2021-10-04 | 0000-00-00 | No | No | Current |