Fosinopril sodium
- Product NDC
- 50090-3780
- 11-digit product format
- 500903780
- Labeler code
- 50090
- Product ID
- 50090-3780_f52be567-3bc8-44f9-a72d-076030284d6a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- fosinopirl sodium
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA205670
- Marketing category
- ANDA
- Marketing start
- 2017-10-01
- Marketing end
- 0000-00-00
- Substance
- FOSINOPRIL SODIUM
- Active strength
- 10 mg/1
- Pharmacologic classes
- Angiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA]
- 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 |
|---|
| 50090-3780-0 | Fosinopril sodium | 30 in 1 BOTTLE | TABLET | 30 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-3780 | FOSINOPRIL SODIUM (FOSINOPIRL SODIUM) TABLET [A-S MEDICATION SOLUTIONS] | 3 | Legacy NDC, 1 package rows | 20200122_9ff203c2-b29b-4cdb-9bd3-2eac190dae5c.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 |
|---|
| 50090-3780-0 | 50090378000 | 30 TABLET in 1 BOTTLE (50090-3780-0) | 30 tablet | 2018-11-06 | 0000-00-00 | No | No | Current |