FERROUS SULFATE
- Product NDC
- 50436-5890
- 11-digit product format
- 504365890
- Labeler code
- 50436
- Product ID
- 50436-5890_c15f644b-745d-43fe-9b6e-a14968da24d7
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- IRON SUPPLEMENT
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Unit Dose Services
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2001-02-19
- Marketing end
- 0000-00-00
- Substance
- FERROUS SULFATE
- Active strength
- 325 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 50436-5890-1 | FERROUS SULFATE | 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 |
|---|
| 50436-5890 | FERROUS SULFATE (IRON SUPPLEMENT) TABLET [UNIT DOSE SERVICES] | 2 | Legacy NDC, 1 package rows | 20130520_77b5dab9-fbf2-48b9-8d56-57096cc15dc6.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 50436-5890-1 | 50436589001 | 30 in 1 BOTTLE | Historical |