What is NDC 72162-2575?

72162-2575 is the product NDC for Minocycline Hydrochloride, Minocycline hydrochloride 50 mg/1 tablet, listed with the FDA by Bryant Ranch Prepack. It has 1 package NDC, shown above in 10- and 11-digit form.

Bryant Ranch Prepack, NDC labeler code 72162. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Minocycline Hydrochloride?

116 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Minocycline Hydrochloride NDC 72162-2575

NDC codes

FDA NDC Directory

Product NDC (as listed)72162-2575Labeler and product segments. Claims need a package NDC.

Product NDC at billing width72162-2575Add 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	Copy
72162-2575-1	72162257501	100 TABLET in 1 BOTTLE (72162-2575-1)Marketed from Nov 17, 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): Minocycline Hydrochloride
Generic name (nonproprietary): minocycline hydrochloride
Active ingredients: Minocycline hydrochloride — 50 mg/1
Dosage form: Tablet
Route: Oral
Labeler: Bryant Ranch PrepackNDC labeler code 72162
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 065156
Marketing start: Apr 2, 2015
Listing expires: Dec 31, 2027
Other FDA classes: Decreased Prothrombin Activity (Physiologic effect)Tetracyclines (Chemical structure)
Identifiers: Product ID 72162-2575_67c910ed-204c-4590-a0eb-e3839f088c86SPL ID 67c910ed-204c-4590-a0eb-e3839f088c86SPL set ID bae17358-1180-4ca8-b163-f9a6f4f83a3dRxCUI 207362UNII 0020414E5U
Pharmacologic class: Tetracycline-class Drug

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

N472162257501 followed by a unit qualifier and the quantity

Package 72162-2575-01. 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 Apr 9, 2026.

Indications (excerpt from the label)

INDICATIONS AND USAGE Minocycline hydrochloride tablets, USP are indicated in the treatment of the following infections due to susceptible strains of the designated microorganisms: Rocky Mountain spotted fever, typhus fever and the typhus group, Q fever, rickettsialpox and tick fevers caused by rickettsiae. Respiratory tract infections caused by Mycoplasma pneumoniae. Lymphogranuloma venereum caused by Chlamydia trachomatis. Psittacosis (Ornithosis) due to Chlamydophila psittaci. Trachoma caused by Chlamydia trachomatis , although the infectious agent is not always eliminated, as judged by immunofluorescence. Inclusion conjunctivitis caused by Chlamydia trachomatis. Nongonococcal urethritis,…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 72162-2575

What is NDC 72162-2575?: 72162-2575 is the product NDC for Minocycline Hydrochloride, Minocycline hydrochloride 50 mg/1 tablet, listed with the FDA by Bryant Ranch Prepack. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Minocycline Hydrochloride.
What is the active ingredient?: Minocycline hydrochloride.
Who is the labeler?: Bryant Ranch Prepack, NDC labeler code 72162. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Minocycline Hydrochloride?: 116 other product NDCs are listed under this name. See all Minocycline 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 Minocycline Hydrochloride NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Minocycline Hydrochloride	Minocycline hydrochloride 100 mg/1	CapsuleOral	REMEDYREPACK INC.	70518-4565	70518-4565-00
minocycline hydrochloride	Minocycline hydrochloride 65 mg/1	Tablet, Extended releaseOral	Zydus Pharmaceuticals (USA) Inc.	68382-532	68382-0532-0168382-0532-0568382-0532-06+3 more
minocycline hydrochloride	Minocycline hydrochloride 115 mg/1	Tablet, Extended releaseOral	Zydus Pharmaceuticals (USA) Inc.	68382-534	68382-0534-0168382-0534-0568382-0534-06+3 more
minocycline hydrochloride	Minocycline hydrochloride 55 mg/1	Tablet, Extended releaseOral	Zydus Pharmaceuticals (USA) Inc.	68382-550	68382-0550-0168382-0550-0568382-0550-06+3 more
minocycline hydrochloride	Minocycline hydrochloride 55 mg/1	Tablet, Extended releaseOral	Zydus Lifesciences Limited	70771-1153	70771-1153-0070771-1153-0170771-1153-03+3 more
minocycline hydrochloride	Minocycline hydrochloride 65 mg/1	Tablet, Extended releaseOral	Zydus Lifesciences Limited	70771-1154	70771-1154-0070771-1154-0170771-1154-03+3 more
minocycline hydrochloride	Minocycline hydrochloride 115 mg/1	Tablet, Extended releaseOral	Zydus Lifesciences Limited	70771-1158	70771-1158-0070771-1158-0170771-1158-03+3 more
Minocycline Hydrochloride	Minocycline hydrochloride 100 mg/1	CapsuleOral	Advanced Rx Pharmacy of Tennessee, LLC	80425-0390	80425-0390-0180425-0390-0280425-0390-03
Minocycline hydrochloride	Minocycline hydrochloride 100 mg/1	CapsuleOral	Northwind Health Company, LLC	82868-017	82868-0017-60
Minocycline hydrochloride	Minocycline hydrochloride 100 mg/1	CapsuleOral	Advanced Rx Pharmacy of Tennessee, LLC	80425-0314	80425-0314-0180425-0314-0280425-0314-03

All 117 Minocycline Hydrochloride NDCs

Other NDCs under ANDA 065156

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

FDA NDC Directory listings under ANDA 065156
Product	Strength	Form · route	Labeler	Product NDC
Minocycline Hydrochloride	Minocycline hydrochloride 100 mg/1	TabletOral	Torrent Pharmaceuticals Limited	13668-487
Minocycline Hydrochloride	Minocycline hydrochloride 75 mg/1	TabletOral	Torrent Pharmaceuticals Limited	13668-486
Minocycline Hydrochloride	Minocycline hydrochloride 50 mg/1	TabletOral	Torrent Pharmaceuticals Limited	13668-485