NDC codes

FDA NDC Directory
Product NDC (as listed)70710-1155Labeler and product segments. Claims need a package NDC.
Product NDC at billing width70710-1155Add 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 NDC11-digit (billing)PackageCopy
70710-1155-17071011550170710115501100 CAPSULE in 1 BOTTLE (70710-1155-1)Marketed from Feb 10, 2022
70710-1155-3707101155037071011550330 CAPSULE in 1 BOTTLE (70710-1155-3)Marketed from Feb 10, 2022
70710-1155-57071011550570710115505500 CAPSULE in 1 BOTTLE (70710-1155-5)Marketed from Feb 10, 2022

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 — 50 mg/1
Dosage form
Capsule
Route
Oral
Labeler
Zydus Pharmaceuticals (USA) Inc.NDC labeler code 70710
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 213441
Marketing start
Listing expires
Identifiers
Product ID 70710-1155_eb495cd8-4bb8-40f5-b578-5e5b9d49b772SPL ID eb495cd8-4bb8-40f5-b578-5e5b9d49b772SPL set ID dbe85bdc-17a1-4201-bf48-a52e35d69b68RxCUI 198045, 198046, 198047, 317136UNII 00FN6IH15DUPC 0370710115432, 0370710115531
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

N470710115501 followed by a unit qualifier and the quantity

Package 70710-1155-01. 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 capsules are 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.

Full label on DailyMed (opens in a new tab)

About NDC 70710-1155

What is NDC 70710-1155?
70710-1155 is the product NDC for Nortriptyline Hydrochloride, Nortriptyline hydrochloride 50 mg/1 capsule, listed with the FDA by Zydus Pharmaceuticals (USA) Inc.. It has 3 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?
Zydus Pharmaceuticals (USA) Inc., NDC labeler code 70710. 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.

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

Other Nortriptyline Hydrochloride NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Nortriptyline HydrochlorideNortriptyline hydrochloride 10 mg/1CapsuleOralREMEDYREPACK INC.70518-476670518-4766-00
Nortriptyline HydrochlorideNortriptyline hydrochloride 25 mg/1CapsuleOralCoupler LLC67046-166167046-1661-03
Nortriptyline HydrochlorideNortriptyline hydrochloride 25 mg/1CapsuleOralAmerican Health Packaging60687-91160687-0911-01
Nortriptyline HydrochlorideNortriptyline hydrochloride 10 mg/1CapsuleOralAmerican Health Packaging60687-90060687-0900-01
Nortriptyline HydrochlorideNortriptyline hydrochloride 25 mg/1CapsuleOralSt. Mary's Medical Park Pharmacy60760-90960760-0909-30
Nortriptyline HydrochlorideNortriptyline hydrochloride 10 mg/1CapsuleOralPreferred Pharmaceuticals Inc.68788-890068788-8900-03
Nortriptyline HydrochlorideNortriptyline hydrochloride 25 mg/1CapsuleOralAdvanced Rx of Tennessee, LLC80425-053480425-0534-0180425-0534-0280425-0534-03
Nortriptyline HydrochlorideNortriptyline hydrochloride 50 mg/1CapsuleOralCoupler LLC67046-153067046-1530-03
Nortriptyline HydrochlorideNortriptyline hydrochloride 75 mg/1CapsuleOralREMEDYREPACK INC.70518-428170518-4281-00
Nortriptyline HydrochlorideNortriptyline hydrochloride 10 mg/1CapsuleOralCoupler LLC67046-150067046-1500-03

All 78 Nortriptyline Hydrochloride NDCs

Other NDCs under ANDA 213441

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

FDA NDC Directory listings under ANDA 213441
ProductStrengthForm · routeLabelerProduct NDC
Nortriptyline HydrochlorideNortriptyline hydrochloride 10 mg/1CapsuleOralZydus Pharmaceuticals (USA) Inc.70710-1153
Nortriptyline HydrochlorideNortriptyline hydrochloride 25 mg/1CapsuleOralZydus Pharmaceuticals (USA) Inc.70710-1154
Nortriptyline HydrochlorideNortriptyline hydrochloride 75 mg/1CapsuleOralZydus Pharmaceuticals (USA) Inc.70710-1156
Nortriptyline HydrochlorideNortriptyline hydrochloride 10 mg/1CapsuleOralZydus Lifesciences Limited70771-1612
Nortriptyline HydrochlorideNortriptyline hydrochloride 25 mg/1CapsuleOralZydus Lifesciences Limited70771-1613
Nortriptyline HydrochlorideNortriptyline hydrochloride 50 mg/1CapsuleOralZydus Lifesciences Limited70771-1614
Nortriptyline HydrochlorideNortriptyline hydrochloride 75 mg/1CapsuleOralZydus Lifesciences Limited70771-1615

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