Albuterol Sulfate
- Product NDC
- 68788-0134
- 11-digit product format
- 687880134
- Labeler code
- 68788
- Product ID
- 68788-0134_04d577a3-73ed-40bf-a527-45861bf5b2f1
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Albuterol Sulfate
- Dosage form
- SOLUTION
- Route
- RESPIRATORY (INHALATION)
- Labeler
- Preferred Pharmaceuticals, Inc
- Application
- ANDA074880
- Marketing category
- ANDA
- Marketing start
- 1997-09-17
- Marketing end
- 0000-00-00
- Substance
- ALBUTEROL SULFATE
- Active strength
- 3 mg/3mL
- Pharmacologic classes
- 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