What is NDC 71335-2415?

71335-2415 is the product NDC for Tetracycline Hydrochloride, Tetracycline hydrochloride 250 mg/1 capsule, listed with the FDA by Bryant Ranch Prepack. It has 8 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 Tetracycline Hydrochloride?

21 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Tetracycline Hydrochloride NDC 71335-2415

NDC codes

FDA NDC Directory

Product NDC (as listed)71335-2415Labeler and product segments. Claims need a package NDC.

Product NDC at billing width71335-2415Add 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
71335-2415-1	7133524150171335241501	20 CAPSULE in 1 BOTTLE (71335-2415-1)Marketed from Nov 12, 2024
71335-2415-2	7133524150271335241502	40 CAPSULE in 1 BOTTLE (71335-2415-2)Marketed from Nov 12, 2024
71335-2415-3	7133524150371335241503	60 CAPSULE in 1 BOTTLE (71335-2415-3)Marketed from Nov 12, 2024
71335-2415-4	7133524150471335241504	30 CAPSULE in 1 BOTTLE (71335-2415-4)Marketed from Nov 12, 2024
71335-2415-5	7133524150571335241505	28 CAPSULE in 1 BOTTLE (71335-2415-5)Marketed from Nov 12, 2024
71335-2415-6	7133524150671335241506	112 CAPSULE in 1 BOTTLE (71335-2415-6)Marketed from Nov 12, 2024
71335-2415-7	7133524150771335241507	6 CAPSULE in 1 BOTTLE (71335-2415-7)Marketed from Nov 12, 2024
71335-2415-8	7133524150871335241508	10 CAPSULE in 1 BOTTLE (71335-2415-8)Marketed from Nov 12, 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): Tetracycline Hydrochloride
Generic name (nonproprietary): tetracycline hydrochloride
Active ingredients: Tetracycline hydrochloride — 250 mg/1
Dosage form: Capsule
Route: Oral
Labeler: Bryant Ranch PrepackNDC labeler code 71335
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 210662
Marketing start: Jan 18, 2019
Listing expires: Dec 31, 2026
Other FDA classes: Tetracyclines (Chemical structure)
Identifiers: Product ID 71335-2415_cf243932-ea5b-4599-bfb0-cf85e5c9ab3eSPL ID cf243932-ea5b-4599-bfb0-cf85e5c9ab3eSPL set ID 58e4b5b3-e093-46e7-b28e-a2c4821c5b63RxCUI 198250UNII P6R62377KV
Pharmacologic class: Tetracycline-class Antimicrobial

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

N471335241501 followed by a unit qualifier and the quantity

Package 71335-2415-01. 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 Nov 12, 2024.

Indications (excerpt from the label)

INDICATIONS AND USAGE To reduce the development of drug-resistant bacteria and maintain the effectiveness of tetracycline hydrochloride and other antibacterial drugs, tetracycline hydrochloride should be used only to treat infections that are proven or strongly suspected to be caused by susceptible bacteria. When culture and susceptibility information are available, they should be considered in selecting or modifying antibacterial therapy. In the absence of such data, local epidemiology and susceptibility patterns may contribute to the empiric selection of therapy. Tetracycline is indicated in the treatment of infections caused by susceptible strains of the designated organisms in the condit…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 71335-2415

What is NDC 71335-2415?: 71335-2415 is the product NDC for Tetracycline Hydrochloride, Tetracycline hydrochloride 250 mg/1 capsule, listed with the FDA by Bryant Ranch Prepack. It has 8 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Tetracycline Hydrochloride.
What is the active ingredient?: Tetracycline hydrochloride.
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 Tetracycline Hydrochloride?: 21 other product NDCs are listed under this name. See all Tetracycline 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 Tetracycline Hydrochloride NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Tetracycline Hydrochloride	Tetracycline hydrochloride 500 mg/1	CapsuleOral	Preferred Pharmaceuticals Inc. .	68788-4134	68788-4134-03
Tetracycline Hydrochloride	Tetracycline hydrochloride 500 mg/1	CapsuleOral	Preferred Pharmaceuticals Inc.	68788-8853	68788-8853-03
tetracycline hydrochloride	Tetracycline hydrochloride 250 mg/1	CapsuleOral	Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.	23155-017	23155-0017-01
tetracycline hydrochloride	Tetracycline hydrochloride 500 mg/1	CapsuleOral	Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.	23155-018	23155-0018-01
Tetracycline Hydrochloride	Tetracycline hydrochloride 250 mg/1	Tablet, Film coatedOral	Pharmaka Generics Inc.	82644-087	82644-0087-60
Tetracycline Hydrochloride	Tetracycline hydrochloride 500 mg/1	Tablet, Film coatedOral	Pharmaka Generics Inc.	82644-870	82644-0870-60
Tetracycline Hydrochloride	Tetracycline hydrochloride 250 mg/1	CapsuleOral	Amneal Pharmaceuticals NY LLC	60219-1522	60219-1522-01
Tetracycline Hydrochloride	Tetracycline hydrochloride 500 mg/1	CapsuleOral	Amneal Pharmaceuticals NY LLC	60219-1523	60219-1523-01
Tetracycline Hydrochloride	Tetracycline hydrochloride 250 mg/1	CapsuleOral	Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.	23155-766	23155-0766-01
Tetracycline Hydrochloride	Tetracycline hydrochloride 500 mg/1	CapsuleOral	Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.	23155-767	23155-0767-01

All 22 Tetracycline Hydrochloride NDCs

Other NDCs under ANDA 210662

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

FDA NDC Directory listings under ANDA 210662
Product	Strength	Form · route	Labeler	Product NDC
Tetracycline Hydrochloride	Tetracycline hydrochloride 250 mg/1	CapsuleOral	Breckenridge Pharmaceutical, Inc.	51991-906
Tetracycline Hydrochloride	Tetracycline hydrochloride 500 mg/1	CapsuleOral	Breckenridge Pharmaceutical, Inc.	51991-907
Tetracycline Hydrochloride	Tetracycline hydrochloride 500 mg/1	CapsuleOral	Bryant Ranch Prepack	71335-2141