minocin
Generic: minocycline hydrochloride
Labeler: melinta therapeutics, llcDrug Facts
Product Profile
Brand Name
minocin
Generic Name
minocycline hydrochloride
Labeler
melinta therapeutics, llc
Dosage Form
INJECTION
Routes
Active Ingredients
minocycline hydrochloride 100 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
70842-160
Product ID
70842-160_07795bdf-7c92-445b-8b8b-d22c5c3eae7a
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
NDA
Application Number
NDA050444
Listing Expiration
2026-12-31
Marketing Start
2013-04-19
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
70842160
Hyphenated Format
70842-160
Supplemental Identifiers
RxCUI
UNII
Packaging Origin
Original Packager
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
minocin (source: ndc)
Generic Name
minocycline hydrochloride (source: ndc)
Application Number
NDA050444 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 100 mg/1
Packaging
- 10 VIAL in 1 CARTON (70842-160-10) / 1 INJECTION in 1 VIAL (70842-160-01)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "07795bdf-7c92-445b-8b8b-d22c5c3eae7a", "openfda": {"unii": ["0020414E5U"], "rxcui": ["207358", "317127"], "spl_set_id": ["e415c323-8219-464b-9e3e-72c5a796cdaa"], "manufacturer_name": ["Melinta Therapeutics, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL in 1 CARTON (70842-160-10) / 1 INJECTION in 1 VIAL (70842-160-01)", "package_ndc": "70842-160-10", "marketing_start_date": "20130419"}], "brand_name": "Minocin", "product_id": "70842-160_07795bdf-7c92-445b-8b8b-d22c5c3eae7a", "dosage_form": "INJECTION", "pharm_class": ["Decreased Prothrombin Activity [PE]", "Tetracycline-class Drug [EPC]", "Tetracyclines [CS]"], "product_ndc": "70842-160", "generic_name": "minocycline hydrochloride", "labeler_name": "Melinta Therapeutics, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Minocin", "active_ingredients": [{"name": "MINOCYCLINE HYDROCHLORIDE", "strength": "100 mg/1"}], "application_number": "NDA050444", "marketing_category": "NDA", "marketing_start_date": "20130419", "listing_expiration_date": "20261231"}