minocycline hydrochloride

Generic: minocycline hydrochloride

Labeler: zydus lifesciences limited
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name minocycline hydrochloride
Generic Name minocycline hydrochloride
Labeler zydus lifesciences limited
Dosage Form TABLET, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

minocycline hydrochloride 65 mg/1

Manufacturer
Zydus Lifesciences Limited

Identifiers & Regulatory

Product NDC 70771-1154
Product ID 70771-1154_5f19958c-a2d2-4ef1-accd-17186e623625
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA203553
Listing Expiration 2026-12-31
Marketing Start 2025-06-12

Pharmacologic Class

Classes
decreased prothrombin activity [pe] tetracycline-class drug [epc] tetracyclines [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 707711154
Hyphenated Format 70771-1154

Supplemental Identifiers

RxCUI
629695 629697 629699 858062 858372 1013659 1013662 1013665
UPC
0370771115419 0370771115310 0370771115617 0370771115518 0370771116713 0370771115815 0370771115716 0370771113811
UNII
0020414E5U

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name minocycline hydrochloride (source: ndc)
Generic Name minocycline hydrochloride (source: ndc)
Application Number ANDA203553 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 65 mg/1
source: ndc
Packaging
  • 1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1154-0)
  • 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1154-1)
  • 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1154-3)
  • 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1154-5)
  • 10 BLISTER PACK in 1 CARTON (70771-1154-7) / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
  • 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1154-9)
source: ndc

Packages (6)

70771-1154-0 1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1154-0) 70771-1154-1 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1154-1) 70771-1154-3 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1154-3) 70771-1154-5 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1154-5) 70771-1154-7 10 BLISTER PACK in 1 CARTON (70771-1154-7) / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK 70771-1154-9 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1154-9)

Ingredients (1)

minocycline hydrochloride (65 mg/1)

Linked Drug Pages (1)

minocycline hydrochloride ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "5f19958c-a2d2-4ef1-accd-17186e623625", "openfda": {"upc": ["0370771115419", "0370771115310", "0370771115617", "0370771115518", "0370771116713", "0370771115815", "0370771115716", "0370771113811"], "unii": ["0020414E5U"], "rxcui": ["629695", "629697", "629699", "858062", "858372", "1013659", "1013662", "1013665"], "spl_set_id": ["8bf9cf23-8ffc-401f-981d-4878d694a468"], "manufacturer_name": ["Zydus Lifesciences Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1154-0)", "package_ndc": "70771-1154-0", "marketing_start_date": "20250612"}, {"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1154-1)", "package_ndc": "70771-1154-1", "marketing_start_date": "20250612"}, {"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1154-3)", "package_ndc": "70771-1154-3", "marketing_start_date": "20250612"}, {"sample": false, "description": "500 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1154-5)", "package_ndc": "70771-1154-5", "marketing_start_date": "20250612"}, {"sample": false, "description": "10 BLISTER PACK in 1 CARTON (70771-1154-7)  / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK", "package_ndc": "70771-1154-7", "marketing_start_date": "20250612"}, {"sample": false, "description": "90 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1154-9)", "package_ndc": "70771-1154-9", "marketing_start_date": "20250612"}], "brand_name": "minocycline hydrochloride", "product_id": "70771-1154_5f19958c-a2d2-4ef1-accd-17186e623625", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Decreased Prothrombin Activity [PE]", "Tetracycline-class Drug [EPC]", "Tetracyclines [CS]"], "product_ndc": "70771-1154", "generic_name": "minocycline hydrochloride", "labeler_name": "Zydus Lifesciences Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "minocycline hydrochloride", "active_ingredients": [{"name": "MINOCYCLINE HYDROCHLORIDE", "strength": "65 mg/1"}], "application_number": "ANDA203553", "marketing_category": "ANDA", "marketing_start_date": "20250612", "listing_expiration_date": "20261231"}