Arformoterol Tartrate
- Product NDC
- 70748-257
- 11-digit product format
- 707480257
- Labeler code
- 70748
- Product ID
- 70748-257_c73ec4be-17c1-4184-a43d-03dde0504a4d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Arformoterol Tartrate
- Dosage form
- SOLUTION
- Route
- RESPIRATORY (INHALATION)
- Labeler
- Lupin Pharmaceuticals, Inc.
- Application
- NDA021912
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 2021-06-01
- Marketing end
- 0000-00-00
- Substance
- ARFORMOTEROL TARTRATE
- Active strength
- 15 ug/2mL
- 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
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 |
|---|
| 70748-257-30 | 70748025730 | 30 POUCH in 1 CARTON (70748-257-30) > 1 VIAL, SINGLE-DOSE in 1 POUCH (70748-257-01) > 2 mL in 1 VIAL, SINGLE-DOSE | 30 pouch | 2021-06-01 | 0000-00-00 | No | No | Current |
| 70748-257-60 | 70748025760 | 15 POUCH in 1 CARTON (70748-257-60) > 4 VIAL, SINGLE-DOSE in 1 POUCH (70748-257-04) > 2 mL in 1 VIAL, SINGLE-DOSE | 15 pouch | 2021-06-01 | 0000-00-00 | No | No | Current |