Levalbuterol
- Product NDC
- 70518-2760
- 11-digit product format
- 705182760
- Labeler code
- 70518
- Product ID
- 70518-2760_d6e8466e-7189-d436-e053-2995a90a68f5
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Levalbuterol
- Dosage form
- SOLUTION
- Route
- RESPIRATORY (INHALATION)
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA090297
- Marketing category
- ANDA
- Marketing start
- 2020-05-29
- Marketing end
- 0000-00-00
- Substance
- LEVALBUTEROL HYDROCHLORIDE
- Active strength
- 1 mg/3mL
- Pharmacologic classes
- Adrenergic beta2-Agonists [MoA], beta2-Adrenergic Agonist [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- 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 |
|---|
| 70518-2760-0 | 70518276000 | 6 POUCH in 1 CARTON (70518-2760-0) > 5 VIAL, SINGLE-DOSE in 1 POUCH > 3 mL in 1 VIAL, SINGLE-DOSE | 6 pouch | 2020-05-29 | 0000-00-00 | No | No | Current |