Minocycline Hydrochloride NDC 71335-1237

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

Bryant Ranch Prepack

Product type

Prescription drug

Marketing category

ANDA — Abbreviated New Drug Application (generic)Application ANDA 065470

Marketing start

Mar 11, 2008

Listing expires

Dec 31, 2026

Other FDA classes

Decreased Prothrombin Activity (Physiologic effect)Tetracyclines (Chemical structure)

Identifiers

Product ID 71335-1237_75bd1b9e-6824-41dc-bddb-1affc5d4e4b5SPL ID 75bd1b9e-6824-41dc-bddb-1affc5d4e4b5SPL set ID a6224eeb-25be-4f1d-889f-809aaf338c8cRxCUI 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

N471335123701 followed by a unit qualifier and the quantity Copy

Package 71335-1237-01. 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

Label details couldn’t be retrieved right now. Open the label on DailyMed.

Other NDCs under ANDA 065470

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