Prescription drug · ANDA
Nortriptyline Hydrochloride NDC 51672-4004
Nortriptyline hydrochloride 75 mg/1 · Capsule · Oral · Sun Pharmaceutical Industries, Inc.
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 51672-4004-1 | 5167240040151672400401 | 100 CAPSULE in 1 BOTTLE (51672-4004-1)Marketed from May 8, 2000 | |
| 51672-4004-2 | 5167240040251672400402 | 500 CAPSULE in 1 BOTTLE (51672-4004-2)Marketed from May 8, 2000 | |
| 51672-4004-5 | 5167240040551672400405 | 90 CAPSULE in 1 BOTTLE (51672-4004-5)Marketed from May 8, 2000 | |
| 51672-4004-6 | 5167240040651672400406 | 30 CAPSULE in 1 BOTTLE (51672-4004-6)Marketed from May 8, 2000 |
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)
- Nortriptyline Hydrochloride
- Generic name (nonproprietary)
- nortriptyline hydrochloride
- Active ingredients
- Nortriptyline hydrochloride — 75 mg/1
- Dosage form
- Capsule
- Route
- Oral
- Labeler
- Sun Pharmaceutical Industries, Inc.NDC labeler code 51672
- Product type
- Prescription drug
- Marketing category
- ANDA — Abbreviated New Drug Application (generic)Application ANDA 075520
- Marketing start
- Listing expires
- Identifiers
- Product ID 51672-4004_56a6d4f3-e026-2d59-e063-6394a90a45beSPL ID 56a6d4f3-e026-2d59-e063-6394a90a45beSPL set ID aee2c1a1-d848-4c3b-8c6d-8a4f6ce94c28RxCUI 198045, 198046, 198047, 317136UNII 00FN6IH15DUPC 0351672400415, 0351672400316, 0351672400118
- 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
N451672400401followed by a unit qualifier and the quantityPackage 51672-4004-01. 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 . This label includes a boxed warning.
Indications (excerpt from the label)
INDICATIONS AND USAGE Nortriptyline hydrochloride is indicated for the relief of symptoms of depression. Endogenous depressions are more likely to be alleviated than are other depressive states.
Excerpt only. Read the full label for complete information.
About NDC 51672-4004
- What is NDC 51672-4004?
- 51672-4004 is the product NDC for Nortriptyline Hydrochloride, Nortriptyline hydrochloride 75 mg/1 capsule, listed with the FDA by Sun Pharmaceutical Industries, Inc.. It has 4 package NDCs, shown above in 10- and 11-digit form.
- What drug is associated with this NDC?
- Nortriptyline Hydrochloride.
- What is the active ingredient?
- Nortriptyline hydrochloride.
- Who is the labeler?
- Sun Pharmaceutical Industries, Inc., NDC labeler code 51672. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
- What other NDCs exist for Nortriptyline Hydrochloride?
- 77 other product NDCs are listed under this name. See all Nortriptyline Hydrochloride NDCs.
- Is there a related HCPCS / J-code?
- Not in Med-Code's curated HCPCS directory. See Billing references above.
Related NDCs: other Nortriptyline Hydrochloride products
Other finished products listed under the same name: strengths, forms and labelers.
| Product | Strength | Form · route | Labeler | Product NDC | Package NDCs (11-digit) |
|---|---|---|---|---|---|
| Nortriptyline Hydrochloride | Nortriptyline hydrochloride 10 mg/1 | CapsuleOral | REMEDYREPACK INC. | 70518-4766 | 70518-4766-00 |
| Nortriptyline Hydrochloride | Nortriptyline hydrochloride 25 mg/1 | CapsuleOral | Coupler LLC | 67046-1661 | 67046-1661-03 |
| Nortriptyline Hydrochloride | Nortriptyline hydrochloride 25 mg/1 | CapsuleOral | American Health Packaging | 60687-911 | 60687-0911-01 |
| Nortriptyline Hydrochloride | Nortriptyline hydrochloride 10 mg/1 | CapsuleOral | American Health Packaging | 60687-900 | 60687-0900-01 |
| Nortriptyline Hydrochloride | Nortriptyline hydrochloride 25 mg/1 | CapsuleOral | St. Mary's Medical Park Pharmacy | 60760-909 | 60760-0909-30 |
| Nortriptyline Hydrochloride | Nortriptyline hydrochloride 10 mg/1 | CapsuleOral | Preferred Pharmaceuticals Inc. | 68788-8900 | 68788-8900-03 |
| Nortriptyline Hydrochloride | Nortriptyline hydrochloride 25 mg/1 | CapsuleOral | Advanced Rx of Tennessee, LLC | 80425-0534 | 80425-0534-0180425-0534-0280425-0534-03 |
| Nortriptyline Hydrochloride | Nortriptyline hydrochloride 50 mg/1 | CapsuleOral | Coupler LLC | 67046-1530 | 67046-1530-03 |
| Nortriptyline Hydrochloride | Nortriptyline hydrochloride 75 mg/1 | CapsuleOral | REMEDYREPACK INC. | 70518-4281 | 70518-4281-00 |
| Nortriptyline Hydrochloride | Nortriptyline hydrochloride 10 mg/1 | CapsuleOral | Coupler LLC | 67046-1500 | 67046-1500-03 |
Other NDCs under ANDA 075520
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 |
|---|---|---|---|---|
| Nortriptyline Hydrochloride | Nortriptyline hydrochloride 10 mg/1 | CapsuleOral | A-S Medication Solutions | 50090-0537 |
| Nortriptyline Hydrochloride | Nortriptyline hydrochloride 25 mg/1 | CapsuleOral | Northwind Health Company, LLC | 51655-507 |
| Nortriptyline Hydrochloride | Nortriptyline hydrochloride 10 mg/1 | CapsuleOral | Sun Pharmaceutical Industries, Inc. | 51672-4001 |
| Nortriptyline Hydrochloride | Nortriptyline hydrochloride 25 mg/1 | CapsuleOral | Sun Pharmaceutical Industries, Inc. | 51672-4002 |
| Nortriptyline Hydrochloride | Nortriptyline hydrochloride 50 mg/1 | CapsuleOral | Sun Pharmaceutical Industries, Inc. | 51672-4003 |
| Nortriptyline Hydrochloride | Nortriptyline hydrochloride 50 mg/1 | CapsuleOral | DIRECT RX | 61919-353 |
| Nortriptyline Hydrochloride | Nortriptyline hydrochloride 25 mg/1 | CapsuleOral | Proficient Rx LP | 63187-396 |
| Nortriptyline Hydrochloride | Nortriptyline hydrochloride 10 mg/1 | CapsuleOral | Proficient Rx LP | 63187-715 |
| Nortriptyline Hydrochloride | Nortriptyline hydrochloride 50 mg/1 | CapsuleOral | Proficient Rx LP | 63187-798 |
| Nortriptyline Hydrochloride | Nortriptyline hydrochloride 25 mg/1 | CapsuleOral | NuCare Pharmaceuticals, Inc. | 68071-3211 |
| Nortriptyline Hydrochloride | Nortriptyline hydrochloride 25 mg/1 | CapsuleOral | Bryant Ranch Prepack | 71335-0083 |
| Nortriptyline Hydrochloride | Nortriptyline hydrochloride 50 mg/1 | CapsuleOral | Bryant Ranch Prepack | 71335-0155 |
| Nortriptyline Hydrochloride | Nortriptyline hydrochloride 10 mg/1 | CapsuleOral | Bryant Ranch Prepack | 71335-0426 |
| Nortriptyline Hydrochloride | Nortriptyline hydrochloride 75 mg/1 | CapsuleOral | Bryant Ranch Prepack | 71335-1552 |
| Nortriptyline Hydrochloride | Nortriptyline hydrochloride 10 mg/1 | CapsuleOral | Northwind Health Company, LLC | 82868-023 |