What is NDC 71335-1840?

71335-1840 is the product NDC for Phendimetrazine Tartrate, Phendimetrazine tartrate 35 mg/1 tablet, listed with the FDA by Bryant Ranch Prepack. It has 10 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 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 71335-1840

NDC codes

FDA NDC Directory

Product NDC (as listed)71335-1840Labeler and product segments. Claims need a package NDC.

Product NDC at billing width71335-1840Add 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
71335-1840-0	71335184000	120 TABLET in 1 BOTTLE (71335-1840-0)Marketed from Jan 30, 2025
71335-1840-1	71335184001	30 TABLET in 1 BOTTLE (71335-1840-1)Marketed from Jan 30, 2025
71335-1840-2	71335184002	90 TABLET in 1 BOTTLE (71335-1840-2)Marketed from Jan 30, 2025
71335-1840-3	71335184003	15 TABLET in 1 BOTTLE (71335-1840-3)Marketed from Jan 30, 2025
71335-1840-4	71335184004	60 TABLET in 1 BOTTLE (71335-1840-4)Marketed from Jan 30, 2025
71335-1840-5	71335184005	7 TABLET in 1 BOTTLE (71335-1840-5)Marketed from Jan 30, 2025
71335-1840-6	71335184006	21 TABLET in 1 BOTTLE (71335-1840-6)Marketed from Jan 30, 2025
71335-1840-7	71335184007	42 TABLET in 1 BOTTLE (71335-1840-7)Marketed from Jan 30, 2025
71335-1840-8	71335184008	100 TABLET in 1 BOTTLE (71335-1840-8)Marketed from Jan 30, 2025
71335-1840-9	71335184009	28 TABLET in 1 BOTTLE (71335-1840-9)Marketed from Jan 30, 2025

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): Phendimetrazine Tartrate
Generic name (nonproprietary): phendimetrazine tartrate
Active ingredients: Phendimetrazine tartrate — 35 mg/1
Dosage form: Tablet
Route: Oral
Labeler: Bryant Ranch PrepackNDC labeler code 71335
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 085588
Marketing start: Jul 1, 2018
Listing expires: Dec 31, 2026
DEA schedule: CIII
Other FDA classes: Appetite Suppression (Physiologic effect)Increased Sympathetic Activity (Physiologic effect)
Identifiers: Product ID 71335-1840_629f541a-8b78-48b2-bb97-1b072195dd83SPL ID 629f541a-8b78-48b2-bb97-1b072195dd83SPL set ID 137e5fcd-9536-4fb9-9885-5dfd1127c35aRxCUI 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

N471335184000 followed by a unit qualifier and the quantity

Package 71335-1840-00. 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 Jan 30, 2025.

Indications (excerpt from the label)

INDICATIONS AND USAGE Phendimetrazine tartrate tablets are 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. The limited usefulness of agents of this class (see CLINICAL PHARMACOLOGY ) should be measured against possible risk factors inherent in their use such as those described below.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 71335-1840

What is NDC 71335-1840?: 71335-1840 is the product NDC for Phendimetrazine Tartrate, Phendimetrazine tartrate 35 mg/1 tablet, listed with the FDA by Bryant Ranch Prepack. It has 10 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?: 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 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	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	10702-077	10702-0077-0110702-0077-0310702-0077-10
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 085588

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

FDA NDC Directory listings under ANDA 085588
Product	Strength	Form · route	Labeler	Product NDC
Phendimetrazine Tartrate	Phendimetrazine tartrate 35 mg/1	TabletOral	Bryant Ranch Prepack	63629-2489
Phendimetrazine Tartrate	Phendimetrazine tartrate 35 mg/1	TabletOral	Virtus Pharmaceuticals, LLC	69543-410