What is NDC 71335-3106?

71335-3106 is the product NDC for Imipramine Hydrochloride, Imipramine hydrochloride 10 mg/1 tablet, film coated, listed with the FDA by Bryant Ranch Prepack. It has 2 package NDCs, shown above in 10- and 11-digit form.

Bryant Ranch Prepack, NDC labeler code 71335. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Imipramine Hydrochloride?

30 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Imipramine Hydrochloride NDC 71335-3106

NDC codes

FDA NDC Directory

Product NDC (as listed)71335-3106Labeler and product segments. Claims need a package NDC.

Product NDC at billing width71335-3106Add 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	Copy
71335-3106-1	71335310601	30 TABLET, FILM COATED in 1 BOTTLE (71335-3106-1)Marketed from Mar 16, 2026
71335-3106-2	71335310602	100 TABLET, FILM COATED in 1 BOTTLE (71335-3106-2)Marketed from Mar 16, 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): Imipramine Hydrochloride
Generic name (nonproprietary): imipramine hydrochloride
Active ingredients: Imipramine hydrochloride — 10 mg/1
Dosage form: Tablet, Film coated
Route: Oral
Labeler: Bryant Ranch PrepackNDC labeler code 71335
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 040903
Marketing start: Apr 7, 2016
Listing expires: Dec 31, 2027
Identifiers: Product ID 71335-3106_baeca134-915e-4cfc-93b6-468bd93ff1ffSPL ID baeca134-915e-4cfc-93b6-468bd93ff1ffSPL set ID bcd3b62a-88d4-49eb-b0aa-71e28cf40919RxCUI 835593UNII BKE5Q1J60U
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

N471335310601 followed by a unit qualifier and the quantity

Package 71335-3106-01. 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

Label details couldn’t be retrieved right now. Open the label on DailyMed.

About NDC 71335-3106

What is NDC 71335-3106?: 71335-3106 is the product NDC for Imipramine Hydrochloride, Imipramine hydrochloride 10 mg/1 tablet, film coated, listed with the FDA by Bryant Ranch Prepack. It has 2 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Imipramine Hydrochloride.
What is the active ingredient?: Imipramine hydrochloride.
Who is the labeler?: Bryant Ranch Prepack, NDC labeler code 71335. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Imipramine Hydrochloride?: 30 other product NDCs are listed under this name. See all Imipramine 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 Imipramine Hydrochloride NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Imipramine Hydrochloride	Imipramine hydrochloride 25 mg/1	Tablet, Film coatedOral	Coupler LLC	67046-1564	67046-1564-03
Imipramine Hydrochloride	Imipramine hydrochloride 25 mg/1	Tablet, Film coatedOral	Advanced Rx Pharmacy of Tennessee, LLC	80425-0342	80425-0342-0180425-0342-0280425-0342-03
Imipramine hydrochloride	Imipramine hydrochloride 10 mg/1	Tablet, Film coatedOral	Advanced Rx Pharmacy of Tennessee, LLC	80425-0294	80425-0294-0180425-0294-0280425-0294-03
Imipramine Hydrochloride	Imipramine hydrochloride 25 mg/1	Tablet, Film coatedOral	Key Therapeutics	70868-810	70868-0810-10
Imipramine Hydrochloride	Imipramine hydrochloride 25 mg/1	TabletOral	Strides Pharma Science Limited	64380-170	64380-0170-0164380-0170-02
Imipramine Hydrochloride	Imipramine hydrochloride 10 mg/1	TabletOral	Strides Pharma Science Limited	64380-169	64380-0169-0164380-0169-02
Imipramine Hydrochloride	Imipramine hydrochloride 50 mg/1	TabletOral	Strides Pharma Science Limited	64380-171	64380-0171-0164380-0171-02
Imipramine Hydrochloride	Imipramine hydrochloride 25 mg/1	TabletOral	REMEDYREPACK INC.	70518-3526	70518-3526-0070518-3526-0170518-3526-03
Imipramine Hydrochloride	Imipramine hydrochloride 50 mg/1	TabletOral	PD-Rx Pharmaceuticals, Inc.	72789-244	72789-0244-01
Imipramine Hydrochloride	Imipramine hydrochloride 10 mg/1	TabletOral	PD-Rx Pharmaceuticals, Inc.	72789-240	72789-0240-0172789-0240-95

All 31 Imipramine Hydrochloride NDCs

Other NDCs under ANDA 040903

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

FDA NDC Directory listings under ANDA 040903
Product	Strength	Form · route	Labeler	Product NDC
Imipramine Hydrochloride	Imipramine hydrochloride 50 mg/1	Tablet, Film coatedOral	REMEDYREPACK INC.	70518-1588
Imipramine Hydrochloride	Imipramine hydrochloride 10 mg/1	Tablet, Film coatedOral	Proficient Rx LP	71205-804
Imipramine Hydrochloride	Imipramine hydrochloride 50 mg/1	Tablet, Film coatedOral	PD-Rx Pharmaceuticals, Inc.	72789-493
Imipramine Hydrochloride	Imipramine hydrochloride 25 mg/1	Tablet, Film coatedOral	PD-Rx Pharmaceuticals, Inc.	72789-492
Imipramine Hydrochloride	Imipramine hydrochloride 25 mg/1	Tablet, Film coatedOral	Bryant Ranch Prepack	71335-2601
Imipramine Hydrochloride	Imipramine hydrochloride 10 mg/1	Tablet, Film coatedOral	Leading Pharma, LLC	69315-133
Imipramine Hydrochloride	Imipramine hydrochloride 25 mg/1	Tablet, Film coatedOral	Leading Pharma, LLC	69315-134
Imipramine Hydrochloride	Imipramine hydrochloride 50 mg/1	Tablet, Film coatedOral	Leading Pharma, LLC	69315-135
Imipramine Hydrochloride	Imipramine hydrochloride 25 mg/1	Tablet, Film coatedOral	A-S Medication Solutions	50090-3148
Imipramine hydrochloride	Imipramine hydrochloride 10 mg/1	Tablet, Film coatedOral	Advanced Rx Pharmacy of Tennessee, LLC	80425-0294
Imipramine Hydrochloride	Imipramine hydrochloride 25 mg/1	Tablet, Film coatedOral	Coupler LLC	67046-1564