Over-the-counter drug · UNAPPROVED HOMEOPATHIC
Thiosinaminum (allylthiourea) NDC 71919-820
Allylthiourea 200 [hp_C]/1 · Pellet · Oral · Washington Homeopathic Products
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 71919-820-01 | 71919082001 | 350 PELLET in 1 VIAL, GLASS (71919-820-01)Marketed from Nov 8, 2023 |
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)
- Thiosinaminum
- Generic name (nonproprietary)
- allylthiourea
- Active ingredients
- Allylthiourea — 200 [hp_C]/1
- Dosage form
- Pellet
- Route
- Oral
- Product type
- Over-the-counter drug
- Marketing category
- Unapproved homeopathic
- Marketing start
- Listing expires
- Identifiers
- Product ID 71919-820_2cc89b36-a4aa-6cac-e063-6394a90a524fSPL ID 2cc89b36-a4aa-6cac-e063-6394a90a524fSPL set ID 09a6cc99-5ebd-5db7-e063-6294a90a80cfUNII 706IDJ14B7
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
N471919082001followed by a unit qualifier and the quantityPackage 71919-0820-01. 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)
INDICATIONS THIOSINAMINUM Scarring
Excerpt only. Read the full label for complete information.