Prescription drug · NDA AUTHORIZED GENERIC
Tretinoin NDC 62032-413
Tretinoin .05 g/100g · Gel · Topical · Obagi Cosmeceuticals LLC
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 62032-413-20 | 62032041320 | 20 g in 1 TUBE (62032-413-20)Marketed from Jun 19, 2014 |
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)
- Tretinoin
- Generic name (nonproprietary)
- tretinoin
- Active ingredients
- Tretinoin — .05 g/100g
- Dosage form
- Gel
- Route
- Topical
- Labeler
- Obagi Cosmeceuticals LLC
- Product type
- Prescription drug
- Marketing category
- NDA authorized genericApplication NDA 022070
- Marketing start
- Listing expires
- Other FDA classes
- Retinoids (Chemical structure)
- Identifiers
- Product ID 62032-413_cf3898ce-f8a0-4e8f-a237-a8d87e3c20a3SPL ID cf3898ce-f8a0-4e8f-a237-a8d87e3c20a3SPL set ID c5ee36ac-2ffd-4cca-ad47-b1dae7ebdb3bRxCUI 245723UNII 5688UTC01R
- Pharmacologic class
- Retinoid
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
N462032041320followed by a unit qualifier and the quantityPackage 62032-0413-20. 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)
Tretinoin Gel is indicated for topical treatment of acne vulgaris. Tretinoin Gel is a retinoid indicated for topical treatment of acne vulgaris. ( 1 )
Excerpt only. Read the full label for complete information.
Other NDCs under NDA 022070
Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.