Fosinopril sodium
- Product NDC
- 53217-277
- 11-digit product format
- 532170277
- Labeler code
- 53217
- Product ID
- 53217-277_537a3cc8-ccd5-4b04-a5a7-3204b7cd07e2
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Fosinopril sodium
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Aidarex Pharmaceuticals LLC
- Application
- ANDA077222
- Marketing category
- ANDA
- Marketing start
- 2005-06-21
- 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
- 2019-12-31
- 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 |
|---|
| 53217-277-30 | Fosinopril sodium | 30 in 1 BOTTLE | TABLET | 30 | | 1 |
| 53217-277-60 | Fosinopril sodium | 60 in 1 BOTTLE | TABLET | 60 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 53217-277 | FOSINOPRIL SODIUM TABLET [AIDAREX PHARMACEUTICALS LLC] | 1 | Legacy NDC, 2 package rows | 20170420_0cef0cd4-e952-40c8-b715-bce4d2f02c51.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 53217-277-30 | 53217027730 | 30 in 1 BOTTLE | Historical |
| 53217-277-60 | 53217027760 | 60 in 1 BOTTLE | Historical |