albuterol sulfate
Generic: albuterol sulfate
Labeler: remedyrepack inc.Drug Facts
Product Profile
Brand Name
albuterol sulfate
Generic Name
albuterol sulfate
Labeler
remedyrepack inc.
Dosage Form
SOLUTION
Routes
Active Ingredients
albuterol sulfate 2.5 mg/3mL
Manufacturer
Identifiers & Regulatory
Product NDC
70518-3442
Product ID
70518-3442_3a99a020-a809-56ec-e063-6394a90a4dd9
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA077839
Listing Expiration
2026-12-31
Marketing Start
2022-06-23
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
705183442
Hyphenated Format
70518-3442
Supplemental Identifiers
RxCUI
UNII
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
albuterol sulfate (source: ndc)
Generic Name
albuterol sulfate (source: ndc)
Application Number
ANDA077839 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 2.5 mg/3mL
Packaging
- 1 POUCH in 1 CARTON (70518-3442-0) / 25 AMPULE in 1 POUCH / 3 mL in 1 AMPULE
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["RESPIRATORY (INHALATION)"], "spl_id": "3a99a020-a809-56ec-e063-6394a90a4dd9", "openfda": {"unii": ["021SEF3731"], "rxcui": ["630208"], "spl_set_id": ["aa3a49f3-667a-4897-a1b7-f067d025a93c"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "1 POUCH in 1 CARTON (70518-3442-0) / 25 AMPULE in 1 POUCH / 3 mL in 1 AMPULE", "package_ndc": "70518-3442-0", "marketing_start_date": "20220623"}], "brand_name": "Albuterol Sulfate", "product_id": "70518-3442_3a99a020-a809-56ec-e063-6394a90a4dd9", "dosage_form": "SOLUTION", "pharm_class": ["Adrenergic beta2-Agonists [MoA]", "beta2-Adrenergic Agonist [EPC]"], "product_ndc": "70518-3442", "generic_name": "Albuterol Sulfate", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Albuterol Sulfate", "active_ingredients": [{"name": "ALBUTEROL SULFATE", "strength": "2.5 mg/3mL"}], "application_number": "ANDA077839", "marketing_category": "ANDA", "marketing_start_date": "20220623", "listing_expiration_date": "20261231"}