Albuterol Sulate
- Product NDC
- 68788-7353
- 11-digit product format
- 687887353
- Labeler code
- 68788
- Product ID
- 68788-7353_a32718c7-20bd-4601-b82b-43b586952fd5
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- albuterol sulfate
- Dosage form
- AEROSOL, METERED
- Route
- RESPIRATORY (INHALATION)
- Labeler
- Preferred Pharmaceuticals Inc.
- Application
- NDA020983
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 2019-02-27
- Marketing end
- 0000-00-00
- Substance
- ALBUTEROL SULFATE
- Active strength
- 90 ug/1
- 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68788-7353-2 | 68788735302 | 1 INHALER in 1 CARTON (68788-7353-2) > 200 AEROSOL, METERED in 1 INHALER | 1 inhaler | 2019-02-27 | 0000-00-00 | No | No | Current |