minocycline hydrochloride NDC 70771-1154

Product information

Brand name (proprietary)

minocycline hydrochloride

Generic name (nonproprietary)

minocycline hydrochloride

Active ingredients

Minocycline hydrochloride — 65 mg/1

Dosage form

Tablet, Extended release

Route

Oral

Labeler

Zydus Lifesciences Limited

Product type

Prescription drug

Marketing category

ANDA — Abbreviated New Drug Application (generic)Application ANDA 203553

Marketing start

Jun 12, 2025

Listing expires

Dec 31, 2026

Other FDA classes

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

Identifiers

Product ID 70771-1154_5f19958c-a2d2-4ef1-accd-17186e623625SPL ID 5f19958c-a2d2-4ef1-accd-17186e623625SPL set ID 8bf9cf23-8ffc-401f-981d-4878d694a468RxCUI 629695, 629697, 629699, 858062, 858372, 1013659, 1013662, 1013665UNII 0020414E5UUPC 0370771115419, 0370771115310, 0370771115617, 0370771115518, 0370771116713, 0370771115815, 0370771115716, 0370771113811

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

N470771115400 followed by a unit qualifier and the quantity Copy

Package 70771-1154-00. 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

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

Other NDCs under ANDA 203553

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