What is NDC 31722-068?

31722-068 is the product NDC for Bupropion hydrochloride, Bupropion hydrochloride 200 mg/1 tablet, extended release, listed with the FDA by Camber Pharmaceuticals, Inc.. It has 4 package NDCs, shown above in 10- and 11-digit form.

Camber Pharmaceuticals, Inc., NDC labeler code 31722. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Bupropion hydrochloride?

171 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Bupropion hydrochloride NDC 31722-068

NDC codes

FDA NDC Directory

Product NDC (as listed)31722-068Labeler and product segments. Claims need a package NDC.

Product NDC at billing width31722-0068Add 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
31722-068-01	3172200680131722006801	100 TABLET, EXTENDED RELEASE in 1 BOTTLE (31722-068-01)Marketed from May 31, 2023
31722-068-05	3172200680531722006805	500 TABLET, EXTENDED RELEASE in 1 BOTTLE (31722-068-05)Marketed from May 31, 2023
31722-068-60	3172200686031722006860	60 TABLET, EXTENDED RELEASE in 1 BOTTLE (31722-068-60)Marketed from May 31, 2023
31722-068-90	3172200689031722006890	90 TABLET, EXTENDED RELEASE in 1 BOTTLE (31722-068-90)Marketed from May 31, 2023

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): Bupropion hydrochloride
Generic name (nonproprietary): bupropion hydrochloride
Active ingredients: Bupropion hydrochloride — 200 mg/1
Dosage form: Tablet, Extended release
Route: Oral
Labeler: Camber Pharmaceuticals, Inc.NDC labeler code 31722
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 216800
Marketing start: May 31, 2023
Listing expires: Dec 31, 2027
Other FDA classes: Dopamine Uptake Inhibitors (Mechanism)Increased Dopamine Activity (Physiologic effect)Increased Norepinephrine Activity (Physiologic effect)Norepinephrine Uptake Inhibitors (Mechanism)
Identifiers: Product ID 31722-068_4daf04dc-4a68-9ce5-e063-6294a90a7033SPL ID 4daf04dc-4a68-9ce5-e063-6294a90a7033SPL set ID f69b322b-93ab-407a-bf25-fe13c6896ca6RxCUI 993503, 993518, 993536UNII ZG7E5POY8O
Pharmacologic class: Aminoketone

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

N431722006801 followed by a unit qualifier and the quantity

Package 31722-0068-01. 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 Mar 23, 2026. This label includes a boxed warning.

Indications (excerpt from the label)

Bupropion hydrochloride extended-release tablets (SR) are indicated for the treatment of major depressive disorder (MDD), as defined by the Diagnostic and Statistical Manual (DSM). The efficacy of bupropion in the treatment of a major depressive episode was established in two 4-week controlled inpatient trials and one 6-week controlled outpatient trial of adult subjects with MDD [see Clinical Studies (14)] . The efficacy of bupropion hydrochloride extended-release tablets (SR) in maintaining an antidepressant response for up to 44 weeks following 8 weeks of acute treatment was demonstrated in a placebo-controlled trial [see Clinical Studies (14) ]. Bupropion hydrochloride extended-release ta…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 31722-068

What is NDC 31722-068?: 31722-068 is the product NDC for Bupropion hydrochloride, Bupropion hydrochloride 200 mg/1 tablet, extended release, listed with the FDA by Camber Pharmaceuticals, Inc.. It has 4 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Bupropion hydrochloride.
What is the active ingredient?: Bupropion hydrochloride.
Who is the labeler?: Camber Pharmaceuticals, Inc., NDC labeler code 31722. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Bupropion hydrochloride?: 171 other product NDCs are listed under this name. See all Bupropion 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 Bupropion hydrochloride NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Bupropion hydrochloride	Bupropion hydrochloride 300 mg/1	Tablet, Extended releaseOral	REMEDYREPACK INC.	70518-4739	70518-4739-00
Bupropion Hydrochloride	Bupropion hydrochloride 100 mg/1	Tablet, Film coatedOral	Coupler LLC	67046-1143	67046-1143-03
Bupropion Hydrochloride	Bupropion hydrochloride 150 mg/1	Tablet, Film coated, Extended releaseOral	Aurobindo Pharma Limited	59651-511	59651-0511-0559651-0511-3059651-0511-90
Bupropion Hydrochloride	Bupropion hydrochloride 300 mg/1	Tablet, Film coated, Extended releaseOral	Aurobindo Pharma Limited	59651-512	59651-0512-0559651-0512-3059651-0512-90
Bupropion hydrochloride	Bupropion hydrochloride 150 mg/1	Tablet, Extended releaseOral	Coupler LLC	67046-1273	67046-1273-03
Bupropion hydrochloride	Bupropion hydrochloride 300 mg/1	TabletOral	Unit Dose Solutions, Inc.	87441-014	87441-0014-01
bupropion hydrochloride	Bupropion hydrochloride 150 mg/1	Tablet, Extended releaseOral	REMEDYREPACK INC.	70518-4674	70518-4674-0070518-4674-0170518-4674-02
Bupropion Hydrochloride	Bupropion hydrochloride 75 mg/1	Tablet, Film coatedOral	Amici Pharma, Inc.	69292-601	69292-0601-01
Bupropion Hydrochloride	Bupropion hydrochloride 100 mg/1	Tablet, Film coatedOral	Amici Pharma, Inc.	69292-602	69292-0602-01
bupropion Hydrochloride	Bupropion hydrochloride 100 mg/1	TabletOral	Coupler LLC	67046-1672	67046-1672-03

All 172 Bupropion hydrochloride NDCs

Other NDCs under ANDA 216800

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

FDA NDC Directory listings under ANDA 216800
Product	Strength	Form · route	Labeler	Product NDC
Bupropion HCL ER(SR)	Bupropion hydrochloride 100 mg/1	Tablet, Extended releaseOral	DriectRx	72189-676
Bupropion hydrochloride	Bupropion hydrochloride 100 mg/1	Tablet, Extended releaseOral	NCS HealthCare of KY, LLC dba Vangard Labs	0615-8601
Bupropion hydrochloride	Bupropion hydrochloride 150 mg/1	Tablet, Extended releaseOral	NCS HealthCare of KY, LLC dba Vangard Labs	0615-8602
Bupropion hydrochloride	Bupropion hydrochloride 100 mg/1	Tablet, Extended releaseOral	Camber Pharmaceuticals, Inc.	31722-066
Bupropion hydrochloride	Bupropion hydrochloride 150 mg/1	Tablet, Extended releaseOral	Camber Pharmaceuticals, Inc.	31722-067
Bupropion hydrochloride	Bupropion hydrochloride 100 mg/1	Tablet, Extended releaseOral	A-S Medication Solutions	50090-7349
Bupropion hydrochloride	Bupropion hydrochloride 150 mg/1	Tablet, Extended releaseOral	A-S Medication Solutions	50090-7422
Bupropion hydrochloride	Bupropion hydrochloride 150 mg/1	Tablet, Extended releaseOral	A-S Medication Solutions	50090-7423
Bupropion hydrochloride	Bupropion hydrochloride 150 mg/1	Tablet, Extended releaseOral	Coupler LLC	67046-1273
Bupropion hydrochloride	Bupropion hydrochloride 100 mg/1	Tablet, Extended releaseOral	Coupler LLC	67046-1572
Bupropion hydrochloride	Bupropion hydrochloride 150 mg/1	Tablet, Extended releaseOral	Preferred Pharmaceuticals Inc.	68788-8769
Bupropion hydrochloride	Bupropion hydrochloride 150 mg/1	Tablet, Extended releaseOral	REMEDYREPACK INC.	70518-4081
Bupropion hydrochloride	Bupropion hydrochloride 100 mg/1	Tablet, Extended releaseOral	REMEDYREPACK INC.	70518-4093
Bupropion hydrochloride	Bupropion hydrochloride 200 mg/1	Tablet, Extended releaseOral	Bryant Ranch Prepack	71335-2400
Bupropion hydrochloride	Bupropion hydrochloride 150 mg/1	Tablet, Extended releaseOral	Bryant Ranch Prepack	71335-2457
Bupropion hydrochloride	Bupropion hydrochloride 100 mg/1	Tablet, Extended releaseOral	Bryant Ranch Prepack	71335-2496
Bupropion hydrochloride	Bupropion hydrochloride 100 mg/1	Tablet, Extended releaseOral	Bryant Ranch Prepack	71335-2649