What is NDC 46708-315?

46708-315 is the product NDC for Desipramine Hydrochloride, Desipramine hydrochloride 10 mg/1 tablet, film coated, listed with the FDA by Alembic Pharmaceuticals Limited. It has 3 package NDCs, shown above in 10- and 11-digit form.

Alembic Pharmaceuticals Limited, NDC labeler code 46708. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Desipramine Hydrochloride?

37 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Desipramine Hydrochloride NDC 46708-315

NDC codes

FDA NDC Directory

Product NDC (as listed)46708-315Labeler and product segments. Claims need a package NDC.

Product NDC at billing width46708-0315Add the package segment from the table below.

Package NDCs as listed with the FDA, and the 11-digit 5-4-2 form used on claims. The highlighted digit is the added leading zero.
Package NDC	11-digit (billing)	Package
46708-315-30	4670803153046708031530	30 TABLET, FILM COATED in 1 BOTTLE (46708-315-30)Marketed from Jul 8, 2021
46708-315-31	4670803153146708031531	100 TABLET, FILM COATED in 1 BOTTLE (46708-315-31)Marketed from Jul 8, 2021
46708-315-91	4670803159146708031591	1000 TABLET, FILM COATED in 1 BOTTLE (46708-315-91)Marketed from Jul 8, 2021

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 Hydrochloride
Generic name (nonproprietary): desipramine hydrochloride
Active ingredients: Desipramine hydrochloride — 10 mg/1
Dosage form: Tablet, Film coated
Route: Oral
Labeler: Alembic Pharmaceuticals LimitedNDC labeler code 46708
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 209785
Marketing start: Jul 8, 2021
Listing expires: Dec 31, 2027
Identifiers: Product ID 46708-315_878a2586-20af-4f35-8908-82474cc732a3SPL ID 878a2586-20af-4f35-8908-82474cc732a3SPL set ID 8b6d2289-aac9-4007-a73d-c168fd2e1d9eRxCUI 1099288, 1099292, 1099296, 1099300, 1099304, 1099316UNII 1Y58DO4MY1UPC 0346708315306
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

N446708031530 followed by a unit qualifier and the quantity

Package 46708-0315-30. 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 Jan 27, 2023. This label includes a boxed warning.

Indications (excerpt from the label)

INDICATIONS AND USAGE Desipramine hydrochloride tablets, USP are indicated for the treatment of depression.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 46708-315

What is NDC 46708-315?: 46708-315 is the product NDC for Desipramine Hydrochloride, Desipramine hydrochloride 10 mg/1 tablet, film coated, listed with the FDA by Alembic Pharmaceuticals Limited. It has 3 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Desipramine Hydrochloride.
What is the active ingredient?: Desipramine hydrochloride.
Who is the labeler?: Alembic Pharmaceuticals Limited, NDC labeler code 46708. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Desipramine Hydrochloride?: 37 other product NDCs are listed under this name. See all Desipramine Hydrochloride NDCs.
Is there a related HCPCS / J-code?: Not in Med-Code's curated HCPCS directory. See Billing references above.

Other finished products listed under the same name: strengths, forms and labelers.

Other Desipramine Hydrochloride NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Desipramine Hydrochloride	Desipramine hydrochloride 10 mg/1	TabletOral	REMEDYREPACK INC.	70518-4645	70518-4645-00
Desipramine Hydrochloride	Desipramine hydrochloride 25 mg/1	Tablet, Film coatedOral	Alembic Pharmaceuticals Limited	46708-316	46708-0316-3046708-0316-3146708-0316-91
Desipramine Hydrochloride	Desipramine hydrochloride 50 mg/1	Tablet, Film coatedOral	Alembic Pharmaceuticals Limited	46708-317	46708-0317-3046708-0317-3146708-0317-91
Desipramine Hydrochloride	Desipramine hydrochloride 75 mg/1	Tablet, Film coatedOral	Alembic Pharmaceuticals Limited	46708-318	46708-0318-3046708-0318-3146708-0318-91
Desipramine Hydrochloride	Desipramine hydrochloride 100 mg/1	Tablet, Film coatedOral	Alembic Pharmaceuticals Limited	46708-319	46708-0319-3046708-0319-3146708-0319-91
Desipramine Hydrochloride	Desipramine hydrochloride 150 mg/1	Tablet, Film coatedOral	Alembic Pharmaceuticals Limited	46708-320	46708-0320-3046708-0320-3146708-0320-50+1 more
Desipramine Hydrochloride	Desipramine hydrochloride 10 mg/1	Tablet, Film coatedOral	Alembic Pharmaceuticals Inc.	62332-315	62332-0315-3062332-0315-3162332-0315-91
Desipramine Hydrochloride	Desipramine hydrochloride 25 mg/1	Tablet, Film coatedOral	Alembic Pharmaceuticals Inc.	62332-316	62332-0316-3062332-0316-3162332-0316-91
Desipramine Hydrochloride	Desipramine hydrochloride 50 mg/1	Tablet, Film coatedOral	Alembic Pharmaceuticals Inc.	62332-317	62332-0317-3062332-0317-3162332-0317-91
Desipramine Hydrochloride	Desipramine hydrochloride 75 mg/1	Tablet, Film coatedOral	Alembic Pharmaceuticals Inc.	62332-318	62332-0318-3062332-0318-3162332-0318-91

All 38 Desipramine Hydrochloride NDCs

Other NDCs under ANDA 209785

Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.

FDA NDC Directory listings under ANDA 209785
Product	Strength	Form · route	Labeler	Product NDC
Desipramine Hydrochloride	Desipramine hydrochloride 25 mg/1	Tablet, Film coatedOral	Alembic Pharmaceuticals Limited	46708-316
Desipramine Hydrochloride	Desipramine hydrochloride 50 mg/1	Tablet, Film coatedOral	Alembic Pharmaceuticals Limited	46708-317
Desipramine Hydrochloride	Desipramine hydrochloride 75 mg/1	Tablet, Film coatedOral	Alembic Pharmaceuticals Limited	46708-318
Desipramine Hydrochloride	Desipramine hydrochloride 100 mg/1	Tablet, Film coatedOral	Alembic Pharmaceuticals Limited	46708-319
Desipramine Hydrochloride	Desipramine hydrochloride 150 mg/1	Tablet, Film coatedOral	Alembic Pharmaceuticals Limited	46708-320
Desipramine Hydrochloride	Desipramine hydrochloride 10 mg/1	Tablet, Film coatedOral	Alembic Pharmaceuticals Inc.	62332-315
Desipramine Hydrochloride	Desipramine hydrochloride 25 mg/1	Tablet, Film coatedOral	Alembic Pharmaceuticals Inc.	62332-316
Desipramine Hydrochloride	Desipramine hydrochloride 50 mg/1	Tablet, Film coatedOral	Alembic Pharmaceuticals Inc.	62332-317
Desipramine Hydrochloride	Desipramine hydrochloride 75 mg/1	Tablet, Film coatedOral	Alembic Pharmaceuticals Inc.	62332-318
Desipramine Hydrochloride	Desipramine hydrochloride 100 mg/1	Tablet, Film coatedOral	Alembic Pharmaceuticals Inc.	62332-319
Desipramine Hydrochloride	Desipramine hydrochloride 150 mg/1	Tablet, Film coatedOral	Alembic Pharmaceuticals Inc.	62332-320