Albuterol Sulfate
- Product NDC
- 68788-7881
- 11-digit product format
- 687887881
- Labeler code
- 68788
- Product ID
- 68788-7881_342f37f4-99cd-44f8-8653-92fcc1b37008
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Albuterol Sulfate
- Dosage form
- AEROSOL, METERED
- Route
- RESPIRATORY (INHALATION)
- Labeler
- Preferred Pharmaceuticals Inc.
- Application
- NDA020503
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 2021-03-09
- Marketing end
- 0000-00-00
- Substance
- ALBUTEROL SULFATE
- Active strength
- 108 ug/1
- 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 |
|---|
| 68788-7881-2 | 68788788102 | 1 CANISTER in 1 CARTON (68788-7881-2) > 200 AEROSOL, METERED in 1 CANISTER | 1 canister | 2021-03-09 | 0000-00-00 | No | No | Current |