Albuterol Sulfate
- Product NDC
- 70518-1095
- 11-digit product format
- 705181095
- Labeler code
- 70518
- Product ID
- 70518-1095_ac3b6bd9-2b37-3cdd-e053-2995a90acb55
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Albuterol Sulfate
- Dosage form
- SOLUTION
- Route
- INTRABRONCHIAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA077839
- Marketing category
- ANDA
- Marketing start
- 2018-04-03
- 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
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-1095-0 | 70518109500 | 60 VIAL in 1 CARTON (70518-1095-0) > 3 mL in 1 VIAL | 60 vial | 2018-04-03 | 0000-00-00 | No | No | Current |