Albuterol Sulfate
- Product NDC
- 53002-1551
- 11-digit product format
- 530021551
- Labeler code
- 53002
- Product ID
- 53002-1551_9122af83-a3a4-446d-8f2f-1bde40d822de
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Albuterol Sulfate
- Dosage form
- AEROSOL, METERED
- Route
- RESPIRATORY (INHALATION)
- Labeler
- RPK Pharmaceuticals, Inc.
- Application
- NDA021457
- Marketing category
- NDA
- Marketing start
- 2019-01-16
- 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
- 2021-12-31
- 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 |
|---|
| 53002-1551-1 | Albuterol SulfateHFA | 1 in 1 CARTON | AEROSOL, METERED | 1 | | 1 |
| 53002-1551-1 | Albuterol SulfateHFA | 200 in 1 INHALER | AEROSOL, METERED | 200 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 53002-1551 | ALBUTEROL SULFATE HFA (ALBUTEROL SULFATE) AEROSOL, METERED [RPK PHARMACEUTICALS, INC.] | 1 | Legacy NDC, 2 package rows | 20201225_316bbc2f-f21b-4ec8-8f73-92486677d6ac.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 |
|---|
| 53002-1551-1 | 53002155101 | 1 INHALER in 1 CARTON (53002-1551-1) > 200 AEROSOL, METERED in 1 INHALER | 1 inhaler | 2019-01-16 | 0000-00-00 | No | No | Current |