What is NDC 10702-077?

10702-077 is the product NDC for Phendimetrazine Tartrate, Phendimetrazine tartrate 35 mg/1 tablet, listed with the FDA by KVK-TECH, INC. It has 3 package NDCs, shown above in 10- and 11-digit form.

KVK-TECH, INC, NDC labeler code 10702. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Phendimetrazine Tartrate?

19 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Phendimetrazine Tartrate NDC 10702-077

NDC codes

FDA NDC Directory

Product NDC (as listed)10702-077Labeler and product segments. Claims need a package NDC.

Product NDC at billing width10702-0077Add 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
10702-077-01	1070200770110702007701	100 TABLET in 1 BOTTLE (10702-077-01)Marketed from Sep 15, 2010
10702-077-03	1070200770310702007703	30 TABLET in 1 BOTTLE (10702-077-03)Marketed from Sep 15, 2010
10702-077-10	1070200771010702007710	1000 TABLET in 1 BOTTLE (10702-077-10)Marketed from Sep 15, 2010

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): Phendimetrazine Tartrate
Generic name (nonproprietary): phendimetrazine tartrate
Active ingredients: Phendimetrazine tartrate — 35 mg/1
Dosage form: Tablet
Route: Oral
Labeler: KVK-TECH, INCNDC labeler code 10702
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 091042
Marketing start: Sep 15, 2010
Listing expires: Dec 31, 2026
DEA schedule: CIII
Other FDA classes: Appetite Suppression (Physiologic effect)Increased Sympathetic Activity (Physiologic effect)
Identifiers: Product ID 10702-077_289ebb0b-370d-4ea1-e063-6394a90a1752SPL ID 289ebb0b-370d-4ea1-e063-6394a90a1752SPL set ID 07bf3488-09e7-436f-af3f-94c35a7be025RxCUI 979549UNII 6985IP0T80
Pharmacologic class: Sympathomimetic Amine Anorectic

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

N410702007701 followed by a unit qualifier and the quantity

Package 10702-0077-01. 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 Dec 6, 2024.

Indications (excerpt from the label)

INDICATIONS AND USAGE: Phendimetrazine tartrate is indicated in the management of exogenous obesity as a short term adjunct (a few weeks) in a regimen of weight reduction based on caloric restriction in patients with an initial body mass index (BMI) of 30 kg/m 2 or higher who have not responded to appropriate weight reducing regimen (diet and/or exercise) alone. Below is a chart of Body Mass Index (BMI) based on various heights and weights. BMI is calculated by taking the patient’s weight, in kilograms (kg), divided by the patient’s height, in meters (m), squared. Metric conversions are as follows: pounds ÷ 2.2 = kg; inches x 0.0254 = meters. Phendimetrazine tartrate is indicated for use as …

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 10702-077

What is NDC 10702-077?: 10702-077 is the product NDC for Phendimetrazine Tartrate, Phendimetrazine tartrate 35 mg/1 tablet, listed with the FDA by KVK-TECH, INC. It has 3 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Phendimetrazine Tartrate.
What is the active ingredient?: Phendimetrazine tartrate.
Who is the labeler?: KVK-TECH, INC, NDC labeler code 10702. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Phendimetrazine Tartrate?: 19 other product NDCs are listed under this name. See all Phendimetrazine Tartrate 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 Phendimetrazine Tartrate NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Phendimetrazine Tartrate	Phendimetrazine tartrate 105 mg/1	Capsule, Extended releaseOral	Acertis Pharmaceuticals, LLC	72989-409	72989-0409-30
Phendimetrazine Tartrate	Phendimetrazine tartrate 35 mg/1	TabletOral	Preferred Pharmaceuticals Inc.	68788-7236	68788-7236-0168788-7236-0268788-7236-03+1 more
Phendimetrazine Tartrate	Phendimetrazine tartrate 35 mg/1	TabletOral	Bryant Ranch Prepack	63629-2489	63629-2489-01
Phendimetrazine Tartrate	Phendimetrazine tartrate 35 mg/1	TabletOral	Virtus Pharmaceuticals, LLC	69543-410	69543-0410-10
Phendimetrazine Tartrate	Phendimetrazine tartrate 35 mg/1	TabletOral	Bryant Ranch Prepack	71335-1840	71335-1840-0071335-1840-0171335-1840-02+7 more
Phendimetrazine Tartrate	Phendimetrazine tartrate 35 mg/1	TabletOral	Elite Laboratories, Inc	64850-440	64850-0440-0164850-0440-10
Phendimetrazine Tartrate	Phendimetrazine tartrate 35 mg/1	TabletOral	NuCare Pharmaceuticals,Inc.	68071-3509	68071-3509-0168071-3509-0668071-3509-08+1 more
Phendimetrazine Tartrate	Phendimetrazine tartrate 35 mg/1	TabletOral	Bryant Ranch Prepack	72162-2044	72162-2044-0072162-2044-0172162-2044-03+1 more
Phendimetrazine Tartrate	Phendimetrazine tartrate 35 mg/1	TabletOral	KVK-TECH, INC	10702-045	10702-0045-0110702-0045-0310702-0045-10
Phendimetrazine Tartrate	Phendimetrazine tartrate 35 mg/1	TabletOral	KVK-TECH, INC	10702-078	10702-0078-0110702-0078-0310702-0078-10

All 20 Phendimetrazine Tartrate NDCs

Other NDCs under ANDA 091042

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

FDA NDC Directory listings under ANDA 091042
Product	Strength	Form · route	Labeler	Product NDC
Phendimetrazine Tartrate	Phendimetrazine tartrate 35 mg/1	TabletOral	KVK-TECH, INC	10702-045
Phendimetrazine Tartrate	Phendimetrazine tartrate 35 mg/1	TabletOral	KVK-TECH, INC	10702-078
Phendimetrazine Tartrate	Phendimetrazine tartrate 35 mg/1	TabletOral	Calvin Scott & Co., Inc.	17224-800
Phendimetrazine Tartrate	Phendimetrazine tartrate 35 mg/1	TabletOral	PD-Rx Pharmaceuticals, Inc.	43063-510
Phendimetrazine Tartrate	Phendimetrazine tartrate 35 mg/1	TabletOral	A-S Medication Solutions	50090-0715
Phendimetrazine Tartrate	Phendimetrazine tartrate 35 mg/1	TabletOral	A-S Medication Solutions	50090-2235
Phendimetrazine Tartrate	Phendimetrazine tartrate 35 mg/1	TabletOral	A-S Medication Solutions	50090-6552
Phendimetrazine Tartrate	Phendimetrazine tartrate 35 mg/1	TabletOral	NuCare Pharmaceuticals, Inc,	66267-394
Phendimetrazine Tartrate	Phendimetrazine tartrate 35 mg/1	TabletOral	NuCare Pharmaceuticals, Inc.	68071-3839
Phendimetrazine Tartrate	Phendimetrazine tartrate 35 mg/1	TabletOral	Preferred Pharmaceuticals Inc.	68788-7236
Phendimetrazine Tartrate	Phendimetrazine tartrate 35 mg/1	TabletOral	Bryant Ranch Prepack	71335-0074
Phendimetrazine Tartrate	Phendimetrazine tartrate 35 mg/1	TabletOral	Bryant Ranch Prepack	71335-0324