What is NDC 72162-1839?

72162-1839 is the product NDC for Minocycline Hydrochloride, Minocycline hydrochloride 80 mg/1 tablet, film coated, extended release, 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?

118 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 72162-1839

NDC codes

FDA NDC Directory

Product NDC (as listed)72162-1839Labeler and product segments. Claims need a package NDC.

Product NDC at billing width72162-1839Add 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
72162-1839-3	7216218390372162183903	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72162-1839-3)Marketed from Sep 30, 2016

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 — 80 mg/1
Dosage form: Tablet, Film coated, Extended release
Route: Oral
Labeler: Bryant Ranch PrepackNDC labeler code 72162
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 204453
Marketing start: Sep 30, 2016
Listing expires: Dec 31, 2027
Other FDA classes: Decreased Prothrombin Activity (Physiologic effect)Tetracyclines (Chemical structure)
Identifiers: Product ID 72162-1839_406aad31-ccfc-4616-a576-dfcdebd065a4SPL ID 406aad31-ccfc-4616-a576-dfcdebd065a4SPL set ID a16012ce-5754-4177-bfb7-dcce696a7189RxCUI 1013665UNII 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

N472162183903 followed by a unit qualifier and the quantity

Package 72162-1839-03. 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 25, 2026.

Indications (excerpt from the label)

Minocycline hydrochloride extended-release tablets is indicated to treat inflammatory lesions of non-nodular moderate to severe acne vulgaris in patients 12 years of age and older. Limitations of Use Minocycline hydrochloride extended-release tablets did not demonstrate any effect on non-inflammatory acne lesions. This formulation of minocycline has not been evaluated in the treatment of infections [see Clinical Studies ( 14 )]. To reduce the development of drug-resistant bacteria as well as to maintain the effectiveness of other antibacterial drugs, use minocycline hydrochloride extended-release tablets only as indicated [see Warnings and Precautions ( 5.12 )]. Minocycline hydrochloride ext…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 72162-1839

What is NDC 72162-1839?: 72162-1839 is the product NDC for Minocycline Hydrochloride, Minocycline hydrochloride 80 mg/1 tablet, film coated, extended release, 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?: 118 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 119 Minocycline Hydrochloride NDCs

Other NDCs under ANDA 204453

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

FDA NDC Directory listings under ANDA 204453
Product	Strength	Form · route	Labeler	Product NDC
Minocycline Hydrochloride	Minocycline hydrochloride 55 mg/1	Tablet, Film coated, Extended releaseOral	Ascend Laboratories, LLC	67877-436
Minocycline Hydrochloride	Minocycline hydrochloride 80 mg/1	Tablet, Film coated, Extended releaseOral	Ascend Laboratories, LLC	67877-437
Minocycline Hydrochloride	Minocycline hydrochloride 105 mg/1	Tablet, Film coated, Extended releaseOral	Ascend Laboratories, LLC	67877-438
Minocycline Hydrochloride	Minocycline hydrochloride 90 mg/1	Tablet, Film coated, Extended releaseOral	PD-Rx Pharmaceuticals, Inc.	72789-525
Minocycline Hydrochloride	Minocycline hydrochloride 45 mg/1	Tablet, Film coated, Extended releaseOral	PD-Rx Pharmaceuticals, Inc.	72789-523
Minocycline Hydrochloride	Minocycline hydrochloride 65 mg/1	Tablet, Film coated, Extended releaseOral	PD-Rx Pharmaceuticals, Inc.	72789-524
Minocycline Hydrochloride	Minocycline hydrochloride 115 mg/1	Tablet, Film coated, Extended releaseOral	PD-Rx Pharmaceuticals, Inc.	72789-529
Minocycline Hydrochloride	Minocycline hydrochloride 55 mg/1	Tablet, Film coated, Extended releaseOral	PD-Rx Pharmaceuticals, Inc.	72789-526
Minocycline Hydrochloride	Minocycline hydrochloride 80 mg/1	Tablet, Film coated, Extended releaseOral	PD-Rx Pharmaceuticals, Inc.	72789-527
Minocycline Hydrochloride	Minocycline hydrochloride 105 mg/1	Tablet, Film coated, Extended releaseOral	PD-Rx Pharmaceuticals, Inc.	72789-528
Minocycline Hydrochloride	Minocycline hydrochloride 105 mg/1	Tablet, Film coated, Extended releaseOral	Bryant Ranch Prepack	63629-9208
Minocycline Hydrochloride	Minocycline hydrochloride 105 mg/1	Tablet, Film coated, Extended releaseOral	Bryant Ranch Prepack	71335-2904
Minocycline Hydrochloride	Minocycline hydrochloride 135 mg/1	Tablet, Film coated, Extended releaseOral	PD-Rx Pharmaceuticals, Inc.	72789-530
Minocycline Hydrochloride	Minocycline hydrochloride 55 mg/1	Tablet, Film coated, Extended releaseOral	Bryant Ranch Prepack	63629-9212
Minocycline Hydrochloride	Minocycline hydrochloride 115 mg/1	Tablet, Film coated, Extended releaseOral	Bryant Ranch Prepack	63629-9209
Minocycline Hydrochloride	Minocycline hydrochloride 135 mg/1	Tablet, Film coated, Extended releaseOral	Bryant Ranch Prepack	63629-9210
Minocycline Hydrochloride	Minocycline hydrochloride 45 mg/1	Tablet, Film coated, Extended releaseOral	Bryant Ranch Prepack	63629-9211
Minocycline Hydrochloride	Minocycline hydrochloride 65 mg/1	Tablet, Film coated, Extended releaseOral	Bryant Ranch Prepack	63629-9213
Minocycline Hydrochloride	Minocycline hydrochloride 80 mg/1	Tablet, Film coated, Extended releaseOral	Bryant Ranch Prepack	63629-9214
Minocycline Hydrochloride	Minocycline hydrochloride 90 mg/1	Tablet, Film coated, Extended releaseOral	Bryant Ranch Prepack	63629-9215

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