Over-the-counter drug · UNAPPROVED DRUG OTHER
Ferrous Sulfate NDC 54738-963
Ferrous sulfate 325 mg/1 · Tablet · Oral · Richmond Pharmaceuticals Inc.
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 54738-963-13 | 54738096313 | 100 TABLET in 1 BOTTLE (54738-963-13)Marketed from Nov 5, 2008 |
How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules
Product information
- Brand name (proprietary)
- Ferrous Sulfate
- Generic name (nonproprietary)
- ferrous sulfate
- Active ingredients
- Ferrous sulfate — 325 mg/1
- Dosage form
- Tablet
- Route
- Oral
- Labeler
- Richmond Pharmaceuticals Inc.NDC labeler code 54738
- Product type
- Over-the-counter drug
- Marketing category
- Unapproved drug (other)
- Marketing start
- Listing expires
- Identifiers
- Product ID 54738-963_2a327df7-e75d-8130-e063-6294a90a6e83SPL ID 2a327df7-e75d-8130-e063-6294a90a6e83SPL set ID 5514d582-19b5-4f1e-b794-f790afb8211cRxCUI 310325UNII 39R4TAN1VTUPC 0054738963137
Billing references
What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.
- HCPCS codeNo match
No HCPCS code in Med-Code's directory. Oral products like this are usually dispensed by a pharmacy and billed by NDC.
- NDC on a medical claim
N454738096313followed by a unit qualifier and the quantityPackage 54738-0963-13. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier
Product label
Current FDA label (SPL), effective . This label includes a boxed warning.
Indications (excerpt from the label)
SUGGESTED USE:
Excerpt only. Read the full label for complete information.
About NDC 54738-963
- What is NDC 54738-963?
- 54738-963 is the product NDC for Ferrous Sulfate, Ferrous sulfate 325 mg/1 tablet, listed with the FDA by Richmond Pharmaceuticals Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.
- What drug is associated with this NDC?
- Ferrous Sulfate.
- What is the active ingredient?
- Ferrous sulfate.
- Who is the labeler?
- Richmond Pharmaceuticals Inc., NDC labeler code 54738. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
- What other NDCs exist for Ferrous Sulfate?
- None: this is the only finished product listed under this name.
- Is there a related HCPCS / J-code?
- Not in Med-Code's curated HCPCS directory. See Billing references above.