Fosinopril sodium
- Product NDC
- 71335-1115
- 11-digit product format
- 713351115
- Labeler code
- 71335
- Product ID
- 71335-1115_fc84aca8-11a0-47d6-9069-70ff69377e4b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- fosinopril sodium
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA205670
- Marketing category
- ANDA
- Marketing start
- 2017-10-01
- Marketing end
- 0000-00-00
- Substance
- FOSINOPRIL SODIUM
- Active strength
- 20 mg/1
- Pharmacologic classes
- Angiotensin Converting Enzyme Inhibitor [EPC], Angiotensin-converting Enzyme Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- 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 |
|---|
| 71335-1115-1 | Fosinopril sodium | 30 in 1 BOTTLE | TABLET | 30 | | 100 |
| 71335-1115-2 | Fosinopril sodium | 28 in 1 BOTTLE | TABLET | 28 | | 100 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 71335-1115 | FOSINOPRIL SODIUM TABLET [BRYANT RANCH PREPACK] | 100 | Legacy NDC, 2 package rows | 20220322_d3632783-58b1-4d73-9c35-e13fbb909ff9.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 |
|---|
| 71335-1115-1 | 71335111501 | 30 TABLET in 1 BOTTLE (71335-1115-1) | 30 tablet | 2019-03-04 | 0000-00-00 | No | No | Current |
| 71335-1115-2 | 71335111502 | 28 TABLET in 1 BOTTLE (71335-1115-2) | 28 tablet | 2019-03-04 | 0000-00-00 | No | No | Current |