NDC codes

FDA NDC Directory
Product NDC (as listed)71335-1123Labeler and product segments. Claims need a package NDC.
Product NDC at billing width71335-1123Add 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 NDC11-digit (billing)PackageCopy
71335-1123-0713351123007133511230050 CAPSULE in 1 BOTTLE (71335-1123-0)Marketed from May 2, 2022
71335-1123-1713351123017133511230120 CAPSULE in 1 BOTTLE (71335-1123-1)Marketed from Nov 6, 2019
71335-1123-2713351123027133511230230 CAPSULE in 1 BOTTLE (71335-1123-2)Marketed from Feb 26, 2019
71335-1123-3713351123037133511230328 CAPSULE in 1 BOTTLE (71335-1123-3)Marketed from May 2, 2022
71335-1123-4713351123047133511230460 CAPSULE in 1 BOTTLE (71335-1123-4)Marketed from Nov 18, 2020
71335-1123-57133511230571335112305100 CAPSULE in 1 BOTTLE (71335-1123-5)Marketed from May 2, 2022
71335-1123-6713351123067133511230614 CAPSULE in 1 BOTTLE (71335-1123-6)Marketed from Mar 7, 2019
71335-1123-77133511230771335112307120 CAPSULE in 1 BOTTLE (71335-1123-7)Marketed from May 2, 2022
71335-1123-8713351123087133511230890 CAPSULE in 1 BOTTLE (71335-1123-8)Marketed from May 2, 2022
71335-1123-9713351123097133511230915 CAPSULE in 1 BOTTLE (71335-1123-9)Marketed from May 2, 2022

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 — 100 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 065470
Marketing start
Listing expires
Other FDA classes
Decreased Prothrombin Activity (Physiologic effect)Tetracyclines (Chemical structure)
Identifiers
Product ID 71335-1123_dc18eddf-e652-4d97-acc0-d6ad545c5ad5SPL ID dc18eddf-e652-4d97-acc0-d6ad545c5ad5SPL set ID bb3b9a7e-6724-4c2a-b3cb-236f522b31a8RxCUI 197984UNII 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

N471335112300 followed by a unit qualifier and the quantity

Package 71335-1123-00. 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 .

Indications (excerpt from the label)

INDICATIONS AND USAGE Minocycline hydrochloride capsules, 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 ureth…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 71335-1123

What is NDC 71335-1123?
71335-1123 is the product NDC for Minocycline Hydrochloride, Minocycline hydrochloride 100 mg/1 capsule, 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?
Minocycline Hydrochloride.
What is the active ingredient?
Minocycline 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 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
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Minocycline HydrochlorideMinocycline hydrochloride 100 mg/1CapsuleOralREMEDYREPACK INC.70518-456570518-4565-00
minocycline hydrochlorideMinocycline hydrochloride 65 mg/1Tablet, Extended releaseOralZydus Pharmaceuticals (USA) Inc.68382-53268382-0532-0168382-0532-0568382-0532-06+3 more
minocycline hydrochlorideMinocycline hydrochloride 115 mg/1Tablet, Extended releaseOralZydus Pharmaceuticals (USA) Inc.68382-53468382-0534-0168382-0534-0568382-0534-06+3 more
minocycline hydrochlorideMinocycline hydrochloride 55 mg/1Tablet, Extended releaseOralZydus Pharmaceuticals (USA) Inc.68382-55068382-0550-0168382-0550-0568382-0550-06+3 more
minocycline hydrochlorideMinocycline hydrochloride 55 mg/1Tablet, Extended releaseOralZydus Lifesciences Limited70771-115370771-1153-0070771-1153-0170771-1153-03+3 more
minocycline hydrochlorideMinocycline hydrochloride 65 mg/1Tablet, Extended releaseOralZydus Lifesciences Limited70771-115470771-1154-0070771-1154-0170771-1154-03+3 more
minocycline hydrochlorideMinocycline hydrochloride 115 mg/1Tablet, Extended releaseOralZydus Lifesciences Limited70771-115870771-1158-0070771-1158-0170771-1158-03+3 more
Minocycline HydrochlorideMinocycline hydrochloride 100 mg/1CapsuleOralAdvanced Rx Pharmacy of Tennessee, LLC80425-039080425-0390-0180425-0390-0280425-0390-03
Minocycline hydrochlorideMinocycline hydrochloride 100 mg/1CapsuleOralNorthwind Health Company, LLC82868-01782868-0017-60
Minocycline hydrochlorideMinocycline hydrochloride 100 mg/1CapsuleOralAdvanced Rx Pharmacy of Tennessee, LLC80425-031480425-0314-0180425-0314-0280425-0314-03

All 119 Minocycline Hydrochloride NDCs

Other NDCs under ANDA 065470

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

FDA NDC Directory listings under ANDA 065470
ProductStrengthForm · routeLabelerProduct NDC
Minocycline HydrochlorideMinocycline hydrochloride 75 mg/1CapsuleOralBryant Ranch Prepack71335-2564
Minocycline HydrochlorideMinocycline hydrochloride 50 mg/1CapsuleOralBryant Ranch Prepack71335-1237
Minocycline HydrochlorideMinocycline hydrochloride 100 mg/1CapsuleOralProficient Rx LP71205-272
Minocycline HydrochlorideMinocycline hydrochloride 100 mg/1CapsuleOralPreferred Pharmaceuticals Inc.68788-7052
Minocycline HydrochlorideMinocycline hydrochloride 100 mg/1CapsuleOralNuCare Pharmaceuticals,Inc.68071-2225
Minocycline HydrochlorideMinocycline hydrochloride 100 mg/1CapsuleOralA-S Medication Solutions50090-2579
Minocycline HydrochlorideMinocycline hydrochloride 100 mg/1CapsuleOralREMEDYREPACK INC.70518-1336
Minocycline HydrochlorideMinocycline hydrochloride 100 mg/1CapsuleOralNorthwind Health Company, LLC51655-004
Minocycline HydrochlorideMinocycline hydrochloride 50 mg/1CapsuleOralAurobindo Pharma Limited65862-209
Minocycline HydrochlorideMinocycline hydrochloride 75 mg/1CapsuleOralAurobindo Pharma Limited65862-210
Minocycline HydrochlorideMinocycline hydrochloride 100 mg/1CapsuleOralAurobindo Pharma Limited65862-211
Minocycline HydrochlorideMinocycline hydrochloride 50 mg/1CapsuleOralA-S Medication Solutions50090-3016
Minocycline HydrochlorideMinocycline hydrochloride 100 mg/1CapsuleOralAdvanced Rx Pharmacy of Tennessee, LLC80425-0390

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