Albuterol Sulfate
- Product NDC
- 55700-908
- 11-digit product format
- 557000908
- Labeler code
- 55700
- Product ID
- 55700-908_bfaf2d3b-3440-4d5a-9575-978d90149898
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Albuterol Sulfate
- Dosage form
- AEROSOL, METERED
- Route
- RESPIRATORY (INHALATION)
- Labeler
- Quality Care Products, LLC
- Application
- NDA020503
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 2021-04-15
- 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
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 55700-908 | ALBUTEROL SULFATE AEROSOL, METERED [QUALITY CARE PRODUCTS, LLC] | 3 | Legacy NDC | 20241220_e0111611-820a-4c48-9bf4-091a79526d2a.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 55700-908-67 | 55700090867 | 1 CANISTER in 1 CARTON (55700-908-67) > 200 AEROSOL, METERED in 1 CANISTER | 1 canister | 2021-04-15 | 0000-00-00 | No | No | Current |