Over-the-counter drug · UNAPPROVED HOMEOPATHIC
Sun Pyrite 8X NDC 48951-8433
Ferrous disulfide 8 [hp_X]/g · Powder · Oral · Uriel Pharmacy, Inc
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 48951-8433-4 | 48951843304 | 50 g in 1 BOTTLE (48951-8433-4)Marketed from Sep 1, 2009 |
How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 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)
- Sun Pyrite 8X
- Generic name (nonproprietary)
- sun pyrite 8x
- Active ingredients
- Ferrous disulfide — 8 [hp_X]/g
- Dosage form
- Powder
- Route
- Oral
- Labeler
- Uriel Pharmacy, Inc
- Product type
- Over-the-counter drug
- Marketing category
- Unapproved homeopathic
- Marketing start
- Listing expires
- Identifiers
- Product ID 48951-8433_2eae3f2d-b712-0f50-e063-6294a90a8349SPL ID 2eae3f2d-b712-0f50-e063-6294a90a8349SPL set ID 2eae3f2d-b711-0f50-e063-6294a90a8349UNII 132N09W4PR
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
N448951843304followed by a unit qualifier and the quantityPackage 48951-8433-04. 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 .
Indications (excerpt from the label)
Directions: FOR ORAL USE ONLY.
Excerpt only. Read the full label for complete information.