Albuterol Sulfate
- Product NDC
- 68788-9298
- 11-digit product format
- 687889298
- Labeler code
- 68788
- Product ID
- 68788-9298_3df6e37b-ebaa-4b7f-8234-8646cc35c7fe
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Albuterol Sulfate
- Dosage form
- SOLUTION
- Route
- INTRABRONCHIAL
- Labeler
- Preferred Pharmaceuticals, Inc.
- Application
- ANDA077839
- Marketing category
- ANDA
- Marketing start
- 2015-04-21
- 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
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68788-9298-2 | 68788929802 | 25 VIAL in 1 CARTON (68788-9298-2) > 3 mL in 1 VIAL | 25 vial | 2015-04-21 | 0000-00-00 | No | No | Current |