Albuterol Sulfate
- Product NDC
- 68788-7477
- 11-digit product format
- 687887477
- Labeler code
- 68788
- Product ID
- 68788-7477_2551d5f6-8ded-464f-b68f-a171af00807e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Albuterol Sulfate
- Dosage form
- AEROSOL, METERED
- Route
- RESPIRATORY (INHALATION)
- Labeler
- Preferred Relabeled By: Preferred Pharmaceuticals Inc.
- Application
- NDA021457
- Marketing category
- NDA
- Marketing start
- 2020-02-18
- 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
- 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 |
|---|
| 68788-7477-2 | 68788747702 | 1 INHALER in 1 CARTON (68788-7477-2) > 200 AEROSOL, METERED in 1 INHALER | 1 inhaler | 2020-02-18 | 0000-00-00 | No | No | Current |