Over-the-counter drug · ANDA
Minoxidil Extra Strength for Men (Minoxidil) NDC 72484-097
Minoxidil 5 g/100mL · Spray · Topical · Roman Health Ventures Inc.
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 72484-097-01 | 72484009701 | 3 BOTTLE, SPRAY in 1 CARTON (72484-097-01) / 60 mL in 1 BOTTLE, SPRAYMarketed from Jan 1, 2024 | |
| 72484-097-02 | 72484009702 | 1 BOTTLE, SPRAY in 1 CARTON (72484-097-02) / 60 mL in 1 BOTTLE, SPRAYMarketed from Jan 1, 2024 |
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)
- Minoxidil Extra Strength for MenSuffix: Extra Strength for Men
- Generic name (nonproprietary)
- minoxidil
- Active ingredients
- Minoxidil — 5 g/100mL
- Dosage form
- Spray
- Route
- Topical
- Labeler
- Roman Health Ventures Inc.NDC labeler code 72484
- Product type
- Over-the-counter drug
- Marketing category
- ANDA — Abbreviated New Drug Application (generic)Application ANDA 076239
- Marketing start
- Listing expires
- Other FDA classes
- Arteriolar Vasodilation (Physiologic effect)
- Identifiers
- Product ID 72484-097_2cee657d-0af4-0821-e063-6294a90af06eSPL ID 2cee657d-0af4-0821-e063-6294a90af06eSPL set ID 03738dd6-a42c-0986-e063-6294a90a1cc0RxCUI 1537948UNII 5965120SH1UPC 0810058746580, 0810058746573
- Pharmacologic class
- Arteriolar Vasodilator
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. Topical products like this are usually dispensed by a pharmacy and billed by NDC.
- NDC on a medical claim
N472484009701followed by a unit qualifier and the quantityPackage 72484-0097-01. 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)
1 Bottle Carton Use to regrow hair on the scalp (vertex only, see picture on side of carton) 3 Bottle Carton Use to regrow hair on the scalp (vertex only, see picture on side of carton)
Excerpt only. Read the full label for complete information.
About NDC 72484-097
- What is NDC 72484-097?
- 72484-097 is the product NDC for Minoxidil Extra Strength for Men (minoxidil), Minoxidil 5 g/100mL spray, listed with the FDA by Roman Health Ventures Inc.. It has 2 package NDCs, shown above in 10- and 11-digit form.
- What drug is associated with this NDC?
- Minoxidil Extra Strength for Men (Minoxidil).
- What is the active ingredient?
- Minoxidil.
- Who is the labeler?
- Roman Health Ventures Inc., NDC labeler code 72484. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
- What other NDCs exist for Minoxidil Extra Strength for Men?
- 3 other product NDCs are listed under this name. See all Minoxidil Extra Strength for Men NDCs.
- Is there a related HCPCS / J-code?
- Not in Med-Code's curated HCPCS directory. See Billing references above.
Related NDCs: other Minoxidil Extra Strength for Men products
Other finished products listed under the same name: strengths, forms and labelers.
| Product | Strength | Form · route | Labeler | Product NDC | Package NDCs (11-digit) |
|---|---|---|---|---|---|
| Minoxidil Extra Strength (For Men)minoxidil | Minoxidil 5 g/100mL | LiquidTopical | FlexiGo Inc | 85524-2614 | 85524-2614-02 |
| Minoxidil Extra Strength (For Men)minoxidil | Minoxidil 5 g/100mL | LiquidTopical | FlexiGo Inc | 85524-2615 | 85524-2615-02 |
| Minoxidil Extra Strength for Menminoxidil | Minoxidil 5 g/100mL | SolutionTopical | Roman Health Ventures Inc. | 72484-095 | 72484-0095-0372484-0095-06 |
Other NDCs under ANDA 076239
Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.
Showing 20 of 30.