What is NDC 68788-8717?

68788-8717 is the product NDC for tramadol hydrochloride, Tramadol hydrochloride 50 mg/1 tablet, listed with the FDA by Preferred Pharmaceuticals Inc.. It has 9 package NDCs, shown above in 10- and 11-digit form.

Preferred Pharmaceuticals Inc., NDC labeler code 68788. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for tramadol hydrochloride?

112 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

tramadol hydrochloride NDC 68788-8717

NDC codes

FDA NDC Directory

Product NDC (as listed)68788-8717Labeler and product segments. Claims need a package NDC.

Product NDC at billing width68788-8717Add 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
68788-8717-1	6878887170168788871701	100 TABLET in 1 BOTTLE (68788-8717-1)Marketed from Jul 18, 2024
68788-8717-2	6878887170268788871702	20 TABLET in 1 BOTTLE (68788-8717-2)Marketed from Jul 18, 2024
68788-8717-3	6878887170368788871703	30 TABLET in 1 BOTTLE (68788-8717-3)Marketed from Jul 18, 2024
68788-8717-4	6878887170468788871704	40 TABLET in 1 BOTTLE (68788-8717-4)Marketed from Jul 18, 2024
68788-8717-5	6878887170568788871705	15 TABLET in 1 BOTTLE (68788-8717-5)Marketed from Jul 18, 2024
68788-8717-6	6878887170668788871706	60 TABLET in 1 BOTTLE (68788-8717-6)Marketed from Jul 18, 2024
68788-8717-7	6878887170768788871707	50 TABLET in 1 BOTTLE (68788-8717-7)Marketed from Jul 18, 2024
68788-8717-8	6878887170868788871708	120 TABLET in 1 BOTTLE (68788-8717-8)Marketed from Jul 18, 2024
68788-8717-9	6878887170968788871709	90 TABLET in 1 BOTTLE (68788-8717-9)Marketed from Jul 18, 2024

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): tramadol hydrochloride
Generic name (nonproprietary): tramadol hydrochloride
Active ingredients: Tramadol hydrochloride — 50 mg/1
Dosage form: Tablet
Route: Oral
Labeler: Preferred Pharmaceuticals Inc.NDC labeler code 68788
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 202075
Marketing start: Jul 18, 2024
Listing expires: Dec 31, 2026
DEA schedule: CIV
Other FDA classes: Full Opioid Agonists (Mechanism)
Identifiers: Product ID 68788-8717_12af9122-aed2-461a-b7fc-e48a030d59a8SPL ID 12af9122-aed2-461a-b7fc-e48a030d59a8SPL set ID 05f8e06b-f3eb-4cb2-aee5-bd0b03884178RxCUI 835603UNII 9N7R477WCK
Pharmacologic class: Opioid Agonist

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

N468788871701 followed by a unit qualifier and the quantity

Package 68788-8717-01. 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 Oct 1, 2025. This label includes a boxed warning.

Indications (excerpt from the label)

Tramadol hydrochloride tablets are indicated in adults for the management of pain severe enough to require an opioid analgesic and for which alternative treatments are inadequate. Limitations of Use Because of the risks of addiction, abuse, and misuse with opioids, which can occur at any dosage or duration (), reserve tramadol hydrochloride tablets for use in patients for whom alternative treatment options [e.g., non-opioid analgesics or opioid combination products): • Have not been tolerated, or are not expected to be tolerated, (1) • Have not provided adequate analgesia, or are not expected to provide adequate analgesia (1) Tramadol hydrochloride tablets should not be used for an extended …

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 68788-8717

What is NDC 68788-8717?: 68788-8717 is the product NDC for tramadol hydrochloride, Tramadol hydrochloride 50 mg/1 tablet, listed with the FDA by Preferred Pharmaceuticals Inc.. It has 9 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: tramadol hydrochloride.
What is the active ingredient?: Tramadol hydrochloride.
Who is the labeler?: Preferred Pharmaceuticals Inc., NDC labeler code 68788. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for tramadol hydrochloride?: 112 other product NDCs are listed under this name. See all tramadol 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 tramadol hydrochloride NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Tramadol Hydrochloride	Tramadol hydrochloride 50 mg/1	TabletOral	REMEDYREPACK INC.	70518-4790	70518-4790-00
Tramadol Hydrochloride	Tramadol hydrochloride 25 mg/1	TabletOral	Rising Pharma Holdings, Inc.	64980-717	64980-0717-03
Tramadol Hydrochloride	Tramadol hydrochloride 50 mg/1	Tablet, CoatedOral	Unit Dose Solutions, Inc.	87441-089	87441-0089-01
tramadol hydrochloride	Tramadol hydrochloride 25 mg/1	TabletOral	Strides Pharma Science Limited	64380-778	64380-0778-01
Tramadol Hydrochloride	Tramadol hydrochloride 50 mg/1	Tablet, CoatedOral	REMEDYREPACK INC.	70518-4713	70518-4713-0070518-4713-0170518-4713-02+1 more
tramadol hydrochloride	Tramadol hydrochloride 50 mg/1	TabletOral	Strides Pharma Science Limited	64380-791	64380-0791-0164380-0791-0264380-0791-03
Tramadol Hydrochloride	Tramadol hydrochloride 50 mg/1	TabletOral	Advanced Rx of Tennessee, LLC	80425-0588	80425-0588-0180425-0588-0280425-0588-03+5 more
Tramadol Hydrochloride	Tramadol hydrochloride 50 mg/1	Tablet, CoatedOral	Northwind Health Company, LLC	82868-110	82868-0110-30
Tramadol Hydrochloride	Tramadol hydrochloride 50 mg/1	Tablet, CoatedOral	Coupler LLC	67046-1209	67046-1209-03
Tramadol Hydrochloride	Tramadol hydrochloride 50 mg/1	TabletOral	Preferred Pharmaceuticals Inc.	68788-4114	68788-4114-0168788-4114-0268788-4114-03+5 more

All 113 tramadol hydrochloride NDCs

Other NDCs under ANDA 202075

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

FDA NDC Directory listings under ANDA 202075
Product	Strength	Form · route	Labeler	Product NDC
tramadol hydrochloride	Tramadol hydrochloride 25 mg/1	TabletOral	Strides Pharma Science Limited	64380-778
tramadol hydrochloride	Tramadol hydrochloride 50 mg/1	TabletOral	Strides Pharma Science Limited	64380-791
tramadol hydrochloride	Tramadol hydrochloride 50 mg/1	TabletOral	NuCare Pharmaceuticals, Inc.	68071-3644
tramadol hydrochloride	Tramadol hydrochloride 50 mg/1	TabletOral	NuCare Pharmaceuticals,Inc.	68071-3655
tramadol hydrochloride	Tramadol hydrochloride 50 mg/1	TabletOral	REMEDYREPACK INC.	70518-4248
tramadol hydrochloride	Tramadol hydrochloride 50 mg/1	TabletOral	Bryant Ranch Prepack	71335-2518
tramadol hydrochloride	Tramadol hydrochloride 50 mg/1	TabletOral	Bryant Ranch Prepack	71335-2612
tramadol hydrochloride	Tramadol hydrochloride 50 mg/1	TabletOral	Proficient Rx LP	82804-114
tramadol hydrochloride	Tramadol hydrochloride 50 mg/1	TabletOral	Northwind Health Company, LLC	82868-052