ipratropium bromide and albuterol sulfate
Generic: ipratropium bromide and albuterol sulfate
Labeler: cipla usa inc.Drug Facts
Product Profile
Brand Name
ipratropium bromide and albuterol sulfate
Generic Name
ipratropium bromide and albuterol sulfate
Labeler
cipla usa inc.
Dosage Form
SOLUTION
Routes
Active Ingredients
albuterol sulfate 2.5 mg/3mL, ipratropium bromide .5 mg/3mL
Manufacturer
Identifiers & Regulatory
Product NDC
69097-840
Product ID
69097-840_14b7dfcc-b3a8-4027-9544-8d52ec2aacf3
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA202496
Listing Expiration
2026-12-31
Marketing Start
2020-06-01
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
69097840
Hyphenated Format
69097-840
Supplemental Identifiers
RxCUI
UNII
Packaging Origin
Original Packager
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
ipratropium bromide and albuterol sulfate (source: ndc)
Generic Name
ipratropium bromide and albuterol sulfate (source: ndc)
Application Number
ANDA202496 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 2.5 mg/3mL
- .5 mg/3mL
Packaging
- 30 POUCH in 1 CARTON (69097-840-53) / 1 VIAL in 1 POUCH (69097-840-34) / 3 mL in 1 VIAL
- 2 POUCH in 1 CARTON (69097-840-64) / 30 VIAL in 1 POUCH / 3 mL in 1 VIAL
- 1 POUCH in 1 CARTON (69097-840-87) / 30 VIAL in 1 POUCH / 3 mL in 1 VIAL
Packages (3)
Ingredients (2)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["RESPIRATORY (INHALATION)"], "spl_id": "14b7dfcc-b3a8-4027-9544-8d52ec2aacf3", "openfda": {"unii": ["021SEF3731", "J697UZ2A9J"], "rxcui": ["1437702"], "spl_set_id": ["89d59bd9-c826-413c-8ed9-a1521a0c7cc5"], "manufacturer_name": ["Cipla USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 POUCH in 1 CARTON (69097-840-53) / 1 VIAL in 1 POUCH (69097-840-34) / 3 mL in 1 VIAL", "package_ndc": "69097-840-53", "marketing_start_date": "20200601"}, {"sample": false, "description": "2 POUCH in 1 CARTON (69097-840-64) / 30 VIAL in 1 POUCH / 3 mL in 1 VIAL", "package_ndc": "69097-840-64", "marketing_start_date": "20200601"}, {"sample": false, "description": "1 POUCH in 1 CARTON (69097-840-87) / 30 VIAL in 1 POUCH / 3 mL in 1 VIAL", "package_ndc": "69097-840-87", "marketing_start_date": "20200601"}], "brand_name": "Ipratropium Bromide and Albuterol Sulfate", "product_id": "69097-840_14b7dfcc-b3a8-4027-9544-8d52ec2aacf3", "dosage_form": "SOLUTION", "pharm_class": ["Adrenergic beta2-Agonists [MoA]", "Anticholinergic [EPC]", "Cholinergic Antagonists [MoA]", "beta2-Adrenergic Agonist [EPC]"], "product_ndc": "69097-840", "generic_name": "Ipratropium Bromide and Albuterol Sulfate", "labeler_name": "Cipla USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ipratropium Bromide and Albuterol Sulfate", "active_ingredients": [{"name": "ALBUTEROL SULFATE", "strength": "2.5 mg/3mL"}, {"name": "IPRATROPIUM BROMIDE", "strength": ".5 mg/3mL"}], "application_number": "ANDA202496", "marketing_category": "ANDA", "marketing_start_date": "20200601", "listing_expiration_date": "20261231"}