Over-the-counter drug · UNAPPROVED HOMEOPATHIC
Dhea (dhea (dehydroepiandrosterone)) NDC 43742-0564
Prasterone 6 [hp_X]/mL · Liquid · Oral · Deseret Biologicals, Inc.
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 43742-0564-1 | 43742056401 | 30 mL in 1 BOTTLE, DROPPER (43742-0564-1)Marketed from Jan 19, 2015 |
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)
- Dhea
- Generic name (nonproprietary)
- dhea (dehydroepiandrosterone)
- Active ingredients
- Prasterone — 6 [hp_X]/mL
- Dosage form
- Liquid
- Route
- Oral
- Labeler
- Deseret Biologicals, Inc.
- Product type
- Over-the-counter drug
- Marketing category
- Unapproved homeopathic
- Marketing start
- Listing expires
- Identifiers
- Product ID 43742-0564_a77dc7d0-2782-45e4-ae58-1625a00f9c41SPL ID a77dc7d0-2782-45e4-ae58-1625a00f9c41SPL set ID d6edd874-495c-4eb5-bf3d-72c2ee41fc88UNII 459AG36T1BUPC 0810151880112
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
N443742056401followed by a unit qualifier and the quantityPackage 43742-0564-01. 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)
USES: • For the temporary relief of symptoms including: • fatigue • low energy These statements are based upon homeopathic principles. They have not been reviewed by the Food and Drug Administration.
Excerpt only. Read the full label for complete information.