minocycline hydrochloride

Generic: minocycline hydrochloride

Labeler: major pharamceuticals
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name minocycline hydrochloride
Generic Name minocycline hydrochloride
Labeler major pharamceuticals
Dosage Form CAPSULE
Routes
ORAL
Active Ingredients

minocycline hydrochloride 100 mg/1

Manufacturer
Major Pharamceuticals

Identifiers & Regulatory

Product NDC 0904-6888
Product ID 0904-6888_aed0618f-2e64-4e18-991b-1e38efcf56b2
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA065062
Listing Expiration 2026-12-31
Marketing Start 2015-04-02

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 09046888
Hyphenated Format 0904-6888

Supplemental Identifiers

RxCUI
197984
UNII
0020414E5U

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 ANDA065062 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 100 mg/1
source: ndc
Packaging
  • 50 BLISTER PACK in 1 CARTON (0904-6888-06) / 1 CAPSULE in 1 BLISTER PACK
source: ndc

Packages (1)

Ingredients (1)

minocycline hydrochloride (100 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "aed0618f-2e64-4e18-991b-1e38efcf56b2", "openfda": {"unii": ["0020414E5U"], "rxcui": ["197984"], "spl_set_id": ["fd86ff45-37d0-4501-b9fb-e1836e4a8be4"], "manufacturer_name": ["Major Pharamceuticals"]}, "finished": true, "packaging": [{"sample": false, "description": "50 BLISTER PACK in 1 CARTON (0904-6888-06)  / 1 CAPSULE in 1 BLISTER PACK", "package_ndc": "0904-6888-06", "marketing_start_date": "20150402"}], "brand_name": "Minocycline Hydrochloride", "product_id": "0904-6888_aed0618f-2e64-4e18-991b-1e38efcf56b2", "dosage_form": "CAPSULE", "pharm_class": ["Decreased Prothrombin Activity [PE]", "Tetracycline-class Drug [EPC]", "Tetracyclines [CS]"], "product_ndc": "0904-6888", "generic_name": "Minocycline Hydrochloride", "labeler_name": "Major Pharamceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Minocycline Hydrochloride", "active_ingredients": [{"name": "MINOCYCLINE HYDROCHLORIDE", "strength": "100 mg/1"}], "application_number": "ANDA065062", "marketing_category": "ANDA", "marketing_start_date": "20150402", "listing_expiration_date": "20261231"}