Albuterol Sulfate
- Product NDC
- 68071-4226
- 11-digit product format
- 680714226
- Labeler code
- 68071
- Product ID
- 68071-4226_62823019-08b3-5760-e053-2991aa0abdee
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Albuterol Sulfate
- Dosage form
- SOLUTION
- Route
- INTRABRONCHIAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA077839
- Marketing category
- ANDA
- Marketing start
- 2010-11-04
- 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
- 2020-12-31
- Current FDA listing
- Historical FDA.report record