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NDC 59651-0333-05 Albuterol 2 mg/1 Details
Albuterol 2 mg/1
Albuterol is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Aurobindo Pharma Limited. The primary component is ALBUTEROL SULFATE.
MedlinePlus Drug Summary
Albuterol is used to prevent and treat wheezing, difficulty breathing, chest tightness, and coughing caused by lung diseases such as asthma and chronic obstructive pulmonary disease (COPD; a group of diseases that affect the lungs and airways). Albuterol is in a class of medications called bronchodilators. It works by relaxing and opening the air passages to the lungs to make breathing easier.
Related Packages: 59651-0333-05Last Updated: 12/01/2022
MedLinePlus Full Drug Details: Albuterol
Product Information
| NDC | 59651-0333 |
|---|---|
| Product ID | 59651-333_f89dffb1-5c4b-48aa-90b4-74043fc9b690 |
| Associated GPIs | |
| GCN Sequence Number | n/a |
| GCN Sequence Number Description | n/a |
| HIC3 | n/a |
| HIC3 Description | n/a |
| GCN | n/a |
| HICL Sequence Number | n/a |
| HICL Sequence Number Description | n/a |
| Brand/Generic | n/a |
| Proprietary Name | Albuterol |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | Albuterol |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Dosage Form | TABLET |
| Route | ORAL |
| Active Ingredient Strength | 2 |
| Active Ingredient Units | mg/1 |
| Substance Name | ALBUTEROL SULFATE |
| Labeler Name | Aurobindo Pharma Limited |
| Pharmaceutical Class | Adrenergic beta2-Agonists [MoA], beta2-Adrenergic Agonist [EPC] |
| DEA Schedule | n/a |
| Marketing Category | ANDA |
| Application Number | ANDA213657 |
| Listing Certified Through | 2024-12-31 |
Package
NDC 59651-0333-05 (59651033305)
| NDC Package Code | 59651-333-05 |
|---|---|
| Billing NDC | 59651033305 |
| Package | 500 TABLET in 1 BOTTLE (59651-333-05) |
| Marketing Start Date | 2020-05-14 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |