FERROUS SULFATE
- Product NDC
- 24451-002
- 11-digit product format
- 244510002
- Labeler code
- 24451
- Product ID
- 24451-002_38d13c4f-3921-4676-827d-146202172021
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- FERROUS SULFATE
- Dosage form
- ELIXIR
- Route
- ORAL
- Labeler
- LLC Federal Solutions
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2013-08-12
- Marketing end
- 0000-00-00
- Substance
- FERROUS SULFATE
- Active strength
- 220 mg/5mL
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#