Ipratropium Bromide and Albuterol Sulfate
- Product NDC
- 50090-2567
- 11-digit product format
- 500902567
- Labeler code
- 50090
- Product ID
- 50090-2567_a061bf92-40e5-49af-a296-bbd18c4b7130
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- ipratropium bromide and albuterol sulfate
- Dosage form
- SOLUTION
- Route
- RESPIRATORY (INHALATION)
- Labeler
- A-S Medication Solutions
- Application
- ANDA202496
- Marketing category
- ANDA
- Marketing start
- 2013-05-13
- Marketing end
- 0000-00-00
- Substance
- IPRATROPIUM BROMIDE; ALBUTEROL SULFATE
- Active strength
- 1 mg/3mL; mg/3mL
- Pharmacologic classes
- Anticholinergic [EPC],Cholinergic Antagonists [MoA],Adrenergic beta2-Agonists [MoA],beta2-Adrenergic Agonist [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record