Albuterol Sulfate
- Product NDC
- 63629-8468
- 11-digit product format
- 636298468
- Labeler code
- 63629
- Product ID
- 63629-8468_5b863106-8f46-4b70-a2f1-4e911a836f07
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Albuterol Sulfate
- Dosage form
- AEROSOL, METERED
- Route
- RESPIRATORY (INHALATION)
- Labeler
- Bryant Ranch Prepack
- Application
- NDA020503
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 2019-04-03
- Marketing end
- 2022-12-31
- 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
- 0000-00-00
- 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 |
|---|
| 63629-8468-1 | 63629846801 | 1 CANISTER in 1 CARTON (63629-8468-1) > 200 AEROSOL, METERED in 1 CANISTER | 1 canister | 2021-05-18 | 2022-12-31 | No | No | Current |