minocycline hydrochloride

Generic: minocycline hydrochloride

Labeler: preferred pharmaceuticals inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name minocycline hydrochloride
Generic Name minocycline hydrochloride
Labeler preferred pharmaceuticals inc.
Dosage Form CAPSULE
Routes
ORAL
Active Ingredients

minocycline hydrochloride 100 mg/1

Manufacturer
Preferred Pharmaceuticals Inc.

Identifiers & Regulatory

Product NDC 68788-7052
Product ID 68788-7052_34f81c26-d31d-4ff8-b581-59dc2074f297
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA065470
Listing Expiration 2026-12-31
Marketing Start 2017-11-06

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 687887052
Hyphenated Format 68788-7052

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 ANDA065470 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 100 mg/1
source: ndc
Packaging
  • 14 CAPSULE in 1 BOTTLE (68788-7052-1)
  • 20 CAPSULE in 1 BOTTLE (68788-7052-2)
  • 30 CAPSULE in 1 BOTTLE (68788-7052-3)
source: ndc

Packages (3)

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": "34f81c26-d31d-4ff8-b581-59dc2074f297", "openfda": {"unii": ["0020414E5U"], "rxcui": ["197984"], "spl_set_id": ["caa99901-467c-4e99-b7e9-fbabdf5d118c"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "14 CAPSULE in 1 BOTTLE (68788-7052-1)", "package_ndc": "68788-7052-1", "marketing_start_date": "20171106"}, {"sample": false, "description": "20 CAPSULE in 1 BOTTLE (68788-7052-2)", "package_ndc": "68788-7052-2", "marketing_start_date": "20171106"}, {"sample": false, "description": "30 CAPSULE in 1 BOTTLE (68788-7052-3)", "package_ndc": "68788-7052-3", "marketing_start_date": "20171106"}], "brand_name": "Minocycline Hydrochloride", "product_id": "68788-7052_34f81c26-d31d-4ff8-b581-59dc2074f297", "dosage_form": "CAPSULE", "pharm_class": ["Decreased Prothrombin Activity [PE]", "Tetracycline-class Drug [EPC]", "Tetracyclines [CS]"], "product_ndc": "68788-7052", "generic_name": "Minocycline Hydrochloride", "labeler_name": "Preferred Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Minocycline Hydrochloride", "active_ingredients": [{"name": "MINOCYCLINE HYDROCHLORIDE", "strength": "100 mg/1"}], "application_number": "ANDA065470", "marketing_category": "ANDA", "marketing_start_date": "20171106", "listing_expiration_date": "20261231"}