Ferrous Sulfate
- Product NDC
- 76413-308
- 11-digit product format
- 764130308
- Labeler code
- 76413
- Product ID
- 76413-308_909b743b-50a1-4bb6-afbf-87a8b12157d1
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Ferrous Sulfate
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Central Texas Community Health Centers
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2014-07-01
- 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 |
|---|
| 76413-308-01 | Ferrous Sulfate | 100 in 1 BOTTLE | TABLET, FILM COATED | 100 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 76413-308 | FERROUS SULFATE TABLET, FILM COATED [CENTRAL TEXAS COMMUNITY HEALTH CENTERS] | 1 | Legacy NDC, 1 package rows | 20160408_c57a8573-d5ae-48b2-afb7-bbec2f63afff.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 76413-308-01 | 76413030801 | 100 in 1 BOTTLE | Historical |