Over-the-counter drug · ANDA
Hairmax Womens Minoxidil Hair Growth Treatment Unscented (Minoxidil) NDC 87616-019
Minoxidil 20 mg/mL · Solution · Topical · Hairmax International, LLC
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 87616-019-00 | 8761600190087616001900 | 1 BOTTLE, DROPPER in 1 BOX (87616-019-00) / 60 mL in 1 BOTTLE, DROPPERMarketed from Sep 24, 2026 |
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)
- Hairmax Womens Minoxidil Hair Growth Treatment Unscented
- Generic name (nonproprietary)
- minoxidil
- Active ingredients
- Minoxidil — 20 mg/mL
- Dosage form
- Solution
- Route
- Topical
- Labeler
- Hairmax International, LLCNDC labeler code 87616
- Product type
- Over-the-counter drug
- Marketing category
- ANDA — Abbreviated New Drug Application (generic)Application ANDA 078176
- Marketing start
- Listing expires
- Other FDA classes
- Arteriolar Vasodilation (Physiologic effect)
- Identifiers
- Product ID 87616-019_5cb66719-eae3-9914-e063-6394a90af48bSPL ID 5cb66719-eae3-9914-e063-6394a90af48b
- 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
N487616001900followed by a unit qualifier and the quantityPackage 87616-0019-00. 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
The FDA listing for this product does not reference a label (SPL) set.
About NDC 87616-019
- What is NDC 87616-019?
- 87616-019 is the product NDC for Hairmax Womens Minoxidil Hair Growth Treatment Unscented, Minoxidil 20 mg/mL solution, listed with the FDA by Hairmax International, LLC. It has 1 package NDC, shown above in 10- and 11-digit form.
- What drug is associated with this NDC?
- Hairmax Womens Minoxidil Hair Growth Treatment Unscented (Minoxidil).
- What is the active ingredient?
- Minoxidil.
- Who is the labeler?
- Hairmax International, LLC, NDC labeler code 87616. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
- What other NDCs exist for Hairmax Womens Minoxidil Hair Growth Treatment Unscented?
- 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.
Other NDCs under ANDA 078176
Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.