ALBUTEROL SULFATE
- Product NDC
- 72189-002
- 11-digit product format
- 721890002
- Labeler code
- 72189
- Product ID
- 72189-002_8ee98719-c249-4373-e053-2995a90ae626
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- ALBUTEROL SULFATE
- Dosage form
- SOLUTION
- Route
- INTRABRONCHIAL
- Labeler
- Direct_Rx
- Application
- ANDA077839
- Marketing category
- ANDA
- Marketing start
- 2019-07-30
- Marketing end
- 0000-00-00
- Substance
- ALBUTEROL SULFATE
- Active strength
- 3 mg/3mL
- Pharmacologic classes
- Adrenergic beta2-Agonists [MoA],beta2-Adrenergic Agonist [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- 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 |
|---|
| 72189-002-25 | ALBUTEROL SULFATE | 3 mL in 1 BOTTLE | SOLUTION | 3 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72189-002 | ALBUTEROL SULFATE SOLUTION [DIRECT_RX] | 1 | Legacy NDC, 1 package rows | 20190731_8ee98719-c248-4373-e053-2995a90ae626.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 |
|---|
| 72189-002-25 | 72189000225 | 3 mL in 1 BOTTLE (72189-002-25) | 3 ml | 2019-07-30 | 0000-00-00 | No | No | Current |