Fosinopril Sodium
- Product NDC
- 50436-3138
- 11-digit product format
- 504363138
- Labeler code
- 50436
- Product ID
- 50436-3138_40901a58-57b6-44fe-8f24-7f2b52455724
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Fosinopril Sodium
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Unit Dose Services
- Application
- ANDA077222
- Marketing category
- ANDA
- Marketing start
- 2007-09-17
- 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
- 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 |
|---|
| 50436-3138-1 | Fosinopril Sodium | 30 in 1 BOTTLE | TABLET | 30 | | 2 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50436-3138 | FOSINOPRIL SODIUM TABLET [UNIT DOSE SERVICES] | 2 | Legacy NDC, 1 package rows | 20130522_1cd8aac4-c59a-460d-97d7-ba3b80e0ab82.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 50436-3138-1 | 50436313801 | 30 in 1 BOTTLE | Historical |