NDC codes

FDA NDC Directory
Product NDC (as listed)71335-0046Labeler and product segments. Claims need a package NDC.
Product NDC at billing width71335-0046Add 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
71335-0046-07133500460050 CAPSULE in 1 BOTTLE (71335-0046-0)Marketed from Apr 11, 2024
71335-0046-17133500460120 CAPSULE in 1 BOTTLE (71335-0046-1)Marketed from Jun 19, 2018
71335-0046-27133500460230 CAPSULE in 1 BOTTLE (71335-0046-2)Marketed from May 7, 2018
71335-0046-37133500460328 CAPSULE in 1 BOTTLE (71335-0046-3)Marketed from Sep 5, 2024
71335-0046-47133500460460 CAPSULE in 1 BOTTLE (71335-0046-4)Marketed from May 13, 2020
71335-0046-571335004605100 CAPSULE in 1 BOTTLE (71335-0046-5)Marketed from Sep 5, 2024
71335-0046-67133500460614 CAPSULE in 1 BOTTLE (71335-0046-6)Marketed from Oct 1, 2018
71335-0046-771335004607120 CAPSULE in 1 BOTTLE (71335-0046-7)Marketed from Sep 5, 2024
71335-0046-87133500460890 CAPSULE in 1 BOTTLE (71335-0046-8)Marketed from Apr 27, 2018
71335-0046-97133500460915 CAPSULE in 1 BOTTLE (71335-0046-9)Marketed from Sep 5, 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)
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 065062
Marketing start
Listing expires
Other FDA classes
Decreased Prothrombin Activity (Physiologic effect)Tetracyclines (Chemical structure)
Identifiers
Product ID 71335-0046_d9d591cb-d704-4949-a582-fc5d21373b75SPL ID d9d591cb-d704-4949-a582-fc5d21373b75SPL set ID 65767ae3-b1ed-4492-90f2-703b2c7e0f38RxCUI 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

N471335004600 followed by a unit qualifier and the quantity

Package 71335-0046-00. 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 urethri…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 71335-0046

What is NDC 71335-0046?
71335-0046 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?
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
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 117 Minocycline Hydrochloride NDCs

Other NDCs under ANDA 065062

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

FDA NDC Directory listings under ANDA 065062
ProductStrengthForm · routeLabelerProduct NDC
Minocycline HydrochlorideMinocycline hydrochloride 100 mg/1CapsuleOralMajor Pharamceuticals0904-6888
Minocycline HydrochlorideMinocycline hydrochloride 50 mg/1CapsuleOralTorrent Pharmaceuticals Limited13668-482
Minocycline HydrochlorideMinocycline hydrochloride 75 mg/1CapsuleOralTorrent Pharmaceuticals Limited13668-483
Minocycline HydrochlorideMinocycline hydrochloride 100 mg/1CapsuleOralTorrent Pharmaceuticals Limited13668-484
Minocycline HydrochlorideMinocycline hydrochloride 100 mg/1CapsuleOralPD-Rx Pharmaceuticals, Inc.43063-736
Minocycline HydrochlorideMinocycline hydrochloride 50 mg/1CapsuleOralA-S Medication Solutions50090-2971
Minocycline HydrochlorideMinocycline hydrochloride 100 mg/1CapsuleOralAmerican Health Packaging60687-336
Minocycline hydrochlorideMinocycline hydrochloride 100 mg/1CapsuleOralProficient Rx LP63187-036
Minocycline hydrochlorideMinocycline hydrochloride 50 mg/1CapsuleOralProficient Rx LP63187-450
Minocycline HydrochlorideMinocycline hydrochloride 100 mg/1CapsuleOralProficient Rx LP63187-850
Minocycline HydrochlorideMinocycline hydrochloride 100 mg/1CapsuleOralNuCare Pharmaceuticals,Inc.68071-2866
Minocycline HydrochlorideMinocycline hydrochloride 50 mg/1CapsuleOralNuCare Pharmaceuticals,Inc.68071-3635
Minocycline HydrochlorideMinocycline hydrochloride 50 mg/1CapsuleOralBryant Ranch Prepack72162-2573
Minocycline HydrochlorideMinocycline hydrochloride 100 mg/1CapsuleOralBryant Ranch Prepack72162-2574
Minocycline hydrochlorideMinocycline hydrochloride 100 mg/1CapsuleOralAdvanced Rx Pharmacy of Tennessee, LLC80425-0314

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