Albuterol Sulfate
- Product NDC
- 17856-0740
- 11-digit product format
- 178560740
- Labeler code
- 17856
- Product ID
- 17856-0740_7413d1db-4d86-40b7-9c83-b36e29d4f06b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Albuterol Sulfate
- Dosage form
- SYRUP
- Route
- ORAL
- Labeler
- ATLANTIC BIOLOGICALS CORP.
- Application
- ANDA074749
- Marketing category
- ANDA
- Marketing start
- 1998-01-30
- Marketing end
- 0000-00-00
- Substance
- ALBUTEROL SULFATE
- Active strength
- 2 mg/5mL
- 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
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 17856-0740-3 | Albuterol Sulfate | 5 mL in 1 CUP | SYRUP | 5 | | 4 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 17856-0740 | ALBUTEROL SULFATE SYRUP [ATLANTIC BIOLOGICALS CORP.] | 4 | Legacy NDC, 1 package rows | 20210129_e21e3867-d156-495b-b8b2-36ad813775fa.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 17856-0740-3 | 17856074003 | 5 mL in 1 CUP (17856-0740-3) | 5 ml | 2021-01-28 | 0000-00-00 | No | No | Current |