minocycline hydrochloride
Generic: minocycline hydrochloride
Labeler: preferred pharmaceuticals inc.Drug Facts
Product Profile
Brand Name
minocycline hydrochloride
Generic Name
minocycline hydrochloride
Labeler
preferred pharmaceuticals inc.
Dosage Form
CAPSULE
Routes
Active Ingredients
minocycline hydrochloride 100 mg/1
Manufacturer
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
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
687887052
Hyphenated Format
68788-7052
Supplemental Identifiers
RxCUI
UNII
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
source: ndc
Resolved Composition
Strengths
- 100 mg/1
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)
Packages (3)
Ingredients (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"}