Prescription drug · ANDA
Desipramine Hydrochloride NDC 70518-4645
Desipramine hydrochloride 10 mg/1 · Tablet · Oral · REMEDYREPACK INC.
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 70518-4645-0 | 70518464500 | 50 POUCH in 1 BOX (70518-4645-0) / 1 TABLET in 1 POUCH (70518-4645-1)Marketed from Apr 28, 2026 |
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)
- Desipramine Hydrochloride
- Generic name (nonproprietary)
- desipramine hydrochloride
- Active ingredients
- Desipramine hydrochloride — 10 mg/1
- Dosage form
- Tablet
- Route
- Oral
- Labeler
- REMEDYREPACK INC.
- Product type
- Prescription drug
- Marketing category
- ANDA — Abbreviated New Drug Application (generic)Application ANDA 204963
- Marketing start
- Listing expires
- Identifiers
- Product ID 70518-4645_508a8ae7-c52d-9157-e063-6294a90a2c9cSPL ID 508a8ae7-c52d-9157-e063-6294a90a2c9cSPL set ID dc1601be-e16a-411f-b9b8-01c51abb2441RxCUI 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
N470518464500followed by a unit qualifier and the quantityPackage 70518-4645-00. 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
Current FDA label (SPL), effective . This label includes a boxed warning.
Indications (excerpt from the label)
INDICATIONS AND USAGE Desipramine hydrochloride tablets 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 HCL | Desipramine hydrochloride 10 mg/1 | TabletOral | Direct_Rx | 72189-391 |
| 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 |