Prescription drug · ANDA
Desipramine HCL NDC 72189-391
Desipramine hydrochloride 10 mg/1 · Tablet · Oral · Direct_Rx
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 72189-391-30 | 72189039130 | 30 TABLET in 1 BOTTLE (72189-391-30)Marketed from Nov 16, 2022 |
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)
- Desipramine HCL
- Generic name (nonproprietary)
- desipramine hcl
- Active ingredients
- Desipramine hydrochloride — 10 mg/1
- Dosage form
- Tablet
- Route
- Oral
- Labeler
- Direct_Rx
- Product type
- Prescription drug
- Marketing category
- ANDA — Abbreviated New Drug Application (generic)Application ANDA 204963
- Marketing start
- Listing expires
- Identifiers
- Product ID 72189-391_2c4cdf7a-45d8-784b-e063-6294a90a82b9SPL ID 2c4cdf7a-45d8-784b-e063-6294a90a82b9SPL set ID ed9d2290-9ad9-ecff-e053-2a95a90a5fd6RxCUI 1099288UNII 1Y58DO4MY1
- Pharmacologic class
- Tricyclic Antidepressant
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
N472189039130followed by a unit qualifier and the quantityPackage 72189-0391-30. 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)
Desipramine hydrochloride tablets, USP is indicated for the treatment of depression.
Excerpt only. Read the full label for complete information.
Other NDCs under ANDA 204963
Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.
| Product | Strength | Form · route | Labeler | Product NDC |
|---|---|---|---|---|
| Desipramine Hydrochloride | Desipramine hydrochloride 10 mg/1 | TabletOral | REMEDYREPACK INC. | 70518-4645 |
| Desipramine Hydrochloride | Desipramine hydrochloride 10 mg/1 | TabletOral | Ingenus Pharmaceuticals, LLC | 50742-112 |
| Desipramine Hydrochloride | Desipramine hydrochloride 25 mg/1 | TabletOral | Ingenus Pharmaceuticals, LLC | 50742-113 |
| Desipramine Hydrochloride | Desipramine hydrochloride 150 mg/1 | TabletOral | Ingenus Pharmaceuticals, LLC | 50742-117 |
| Desipramine Hydrochloride | Desipramine hydrochloride 50 mg/1 | TabletOral | Ingenus Pharmaceuticals, LLC | 50742-114 |
| Desipramine Hydrochloride | Desipramine hydrochloride 75 mg/1 | TabletOral | Ingenus Pharmaceuticals, LLC | 50742-115 |
| Desipramine Hydrochloride | Desipramine hydrochloride 100 mg/1 | TabletOral | Ingenus Pharmaceuticals, LLC | 50742-116 |