albuterol sulfate

Generic: albuterol sulfate

Labeler: luoxin aurovitas pharma (chengdu) co., ltd.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name albuterol sulfate
Generic Name albuterol sulfate
Labeler luoxin aurovitas pharma (chengdu) co., ltd.
Dosage Form SOLUTION
Routes
RESPIRATORY (INHALATION)
Active Ingredients

albuterol sulfate .63 mg/3mL

Manufacturer
Luoxin Aurovitas Pharma (Chengdu) Co., Ltd.

Identifiers & Regulatory

Product NDC 81894-105
Product ID 81894-105_1d6bfa3d-ae1f-8167-e063-6394a90a2356
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA211888
Listing Expiration 2026-12-31
Marketing Start 2020-04-20

Pharmacologic Class

Classes
adrenergic beta2-agonists [moa] beta2-adrenergic agonist [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 81894105
Hyphenated Format 81894-105

Supplemental Identifiers

RxCUI
351136 351137
UPC
0381894106055 0381894105058
UNII
021SEF3731

Packaging Origin

Original Packager
true

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 ANDA211888 (source: ndc)
Routes
RESPIRATORY (INHALATION)
source: ndc

Resolved Composition

Strengths
  • .63 mg/3mL
source: ndc
Packaging
  • 5 POUCH in 1 CARTON (81894-105-25) / 5 VIAL in 1 POUCH / 3 mL in 1 VIAL
  • 6 POUCH in 1 CARTON (81894-105-30) / 5 VIAL in 1 POUCH / 3 mL in 1 VIAL
source: ndc

Packages (2)

81894-105-25 5 POUCH in 1 CARTON (81894-105-25) / 5 VIAL in 1 POUCH / 3 mL in 1 VIAL 81894-105-30 6 POUCH in 1 CARTON (81894-105-30) / 5 VIAL in 1 POUCH / 3 mL in 1 VIAL

Ingredients (1)

albuterol sulfate (.63 mg/3mL)

Linked Drug Pages (1)

ALBUTEROL SULFATE ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["RESPIRATORY (INHALATION)"], "spl_id": "1d6bfa3d-ae1f-8167-e063-6394a90a2356", "openfda": {"upc": ["0381894106055", "0381894105058"], "unii": ["021SEF3731"], "rxcui": ["351136", "351137"], "spl_set_id": ["1d6be2b8-c670-b783-e063-6294a90ae503"], "manufacturer_name": ["Luoxin Aurovitas Pharma (Chengdu) Co., Ltd."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "5 POUCH in 1 CARTON (81894-105-25)  / 5 VIAL in 1 POUCH / 3 mL in 1 VIAL", "package_ndc": "81894-105-25", "marketing_start_date": "20200420"}, {"sample": false, "description": "6 POUCH in 1 CARTON (81894-105-30)  / 5 VIAL in 1 POUCH / 3 mL in 1 VIAL", "package_ndc": "81894-105-30", "marketing_start_date": "20240729"}], "brand_name": "ALBUTEROL SULFATE", "product_id": "81894-105_1d6bfa3d-ae1f-8167-e063-6394a90a2356", "dosage_form": "SOLUTION", "pharm_class": ["Adrenergic beta2-Agonists [MoA]", "beta2-Adrenergic Agonist [EPC]"], "product_ndc": "81894-105", "generic_name": "ALBUTEROL SULFATE", "labeler_name": "Luoxin Aurovitas Pharma (Chengdu) Co., Ltd.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "ALBUTEROL SULFATE", "active_ingredients": [{"name": "ALBUTEROL SULFATE", "strength": ".63 mg/3mL"}], "application_number": "ANDA211888", "marketing_category": "ANDA", "marketing_start_date": "20200420", "listing_expiration_date": "20261231"}