What is NDC 71205-086?

71205-086 is the product NDC for Minocycline Hydrochloride, Minocycline hydrochloride 50 mg/1 capsule, listed with the FDA by Proficient Rx LP. It has 5 package NDCs, shown above in 10- and 11-digit form.

Proficient Rx LP, NDC labeler code 71205. 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 71205-086

NDC codes

FDA NDC Directory

Product NDC (as listed)71205-086Labeler and product segments. Claims need a package NDC.

Product NDC at billing width71205-0086Add 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
71205-086-20	71205008620	20 CAPSULE in 1 BOTTLE, PLASTIC (71205-086-20)Marketed from Aug 1, 2018
71205-086-21	71205008621	21 CAPSULE in 1 BOTTLE, PLASTIC (71205-086-21)Marketed from Aug 1, 2018
71205-086-30	71205008630	30 CAPSULE in 1 BOTTLE, PLASTIC (71205-086-30)Marketed from Aug 1, 2018
71205-086-60	71205008660	60 CAPSULE in 1 BOTTLE, PLASTIC (71205-086-60)Marketed from Aug 1, 2018
71205-086-90	71205008690	90 CAPSULE in 1 BOTTLE, PLASTIC (71205-086-90)Marketed from Jan 3, 2022

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): Minocycline Hydrochloride
Generic name (nonproprietary): minocycline hydrochloride
Active ingredients: Minocycline hydrochloride — 50 mg/1
Dosage form: Capsule
Route: Oral
Labeler: Proficient Rx LPNDC labeler code 71205
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 063181
Marketing start: Feb 1, 1992
Listing expires: Dec 31, 2026
Other FDA classes: Tetracyclines (Chemical structure)
Identifiers: Product ID 71205-086_a2baa928-f954-40a1-a0e7-f7e373f5d3ebSPL ID a2baa928-f954-40a1-a0e7-f7e373f5d3ebSPL set ID d5fcba91-6aa6-4072-aea5-fb8da65d9aacRxCUI 197985UNII 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

N471205008620 followed by a unit qualifier and the quantity

Package 71205-0086-20. 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 Sep 1, 2022.

Indications (excerpt from the label)

INDICATIONS AND USAGE Minocycline hydrochloride capsules 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, end…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 71205-086

What is NDC 71205-086?: 71205-086 is the product NDC for Minocycline Hydrochloride, Minocycline hydrochloride 50 mg/1 capsule, listed with the FDA by Proficient Rx LP. It has 5 package NDCs, 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?: Proficient Rx LP, NDC labeler code 71205. 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 063181

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

FDA NDC Directory listings under ANDA 063181
Product	Strength	Form · route	Labeler	Product NDC
Minocycline Hydrochloride	Minocycline hydrochloride 50 mg/1	CapsuleOral	PD-Rx Pharmaceuticals, Inc.	55289-202
Minocycline Hydrochloride	Minocycline hydrochloride 50 mg/1	CapsuleOral	Bryant Ranch Prepack	71335-0682