NDC codes

FDA NDC Directory
Product NDC (as listed)64380-156Labeler and product segments. Claims need a package NDC.
Product NDC at billing width64380-0156Add 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
64380-156-016438001560150 TABLET in 1 BOTTLE (64380-156-01)Marketed from Apr 11, 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 — 100 mg/1
Dosage form
Tablet
Route
Oral
Labeler
Strides Pharma Science LimitedNDC labeler code 64380
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 065131
Marketing start
Listing expires
Other FDA classes
Tetracyclines (Chemical structure)
Identifiers
Product ID 64380-156_73a30dc4-352b-4307-b902-07ffefc99a99SPL ID 73a30dc4-352b-4307-b902-07ffefc99a99SPL set ID d6e136ba-c9b1-4846-ae2a-98a29cb4504dRxCUI 207362, 207364, 403840UNII 0020414E5UUPC 0364380156017, 0364380155010, 0364380154013
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

N464380015601 followed by a unit qualifier and the quantity

Package 64380-0156-01. 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 .

Indications (excerpt from the label)

INDICATIONS AND USAGE Minocycline hydrochloride tablets 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 Chlamydia 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, endocervi…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 64380-156

What is NDC 64380-156?
64380-156 is the product NDC for Minocycline Hydrochloride, Minocycline hydrochloride 100 mg/1 tablet, listed with the FDA by Strides Pharma Science Limited. 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?
Strides Pharma Science Limited, NDC labeler code 64380. 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 065131

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

FDA NDC Directory listings under ANDA 065131
ProductStrengthForm · routeLabelerProduct NDC
Minocycline HydrochlorideMinocycline hydrochloride 50 mg/1TabletOralStrides Pharma Science Limited64380-154
Minocycline HydrochlorideMinocycline hydrochloride 75 mg/1TabletOralStrides Pharma Science Limited64380-155

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