minocycline hydrochloride
Generic: minocycline hydrochloride
Labeler: actavis pharma, inc.Drug Facts
Product Profile
Brand Name
minocycline hydrochloride
Generic Name
minocycline hydrochloride
Labeler
actavis pharma, inc.
Dosage Form
CAPSULE
Routes
Active Ingredients
minocycline hydrochloride 50 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
0591-5694
Product ID
0591-5694_2d74faa2-99c4-4f01-adc6-60110d2b24da
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA063181
Listing Expiration
2026-12-31
Marketing Start
1992-02-01
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
05915694
Hyphenated Format
0591-5694
Supplemental Identifiers
RxCUI
UPC
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
minocycline hydrochloride (source: ndc)
Generic Name
minocycline hydrochloride (source: ndc)
Application Number
ANDA063181 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 50 mg/1
Packaging
- 100 CAPSULE in 1 BOTTLE, PLASTIC (0591-5694-01)
- 60 CAPSULE in 1 BOTTLE, PLASTIC (0591-5694-60)
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2d74faa2-99c4-4f01-adc6-60110d2b24da", "openfda": {"upc": ["0305915694017"], "unii": ["0020414E5U"], "rxcui": ["197984", "197985", "314108"], "spl_set_id": ["a5fc4d50-50b2-46e0-b722-4c6b2ec47d06"], "manufacturer_name": ["Actavis Pharma, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE, PLASTIC (0591-5694-01)", "package_ndc": "0591-5694-01", "marketing_start_date": "19920201"}, {"sample": false, "description": "60 CAPSULE in 1 BOTTLE, PLASTIC (0591-5694-60)", "package_ndc": "0591-5694-60", "marketing_start_date": "20060525"}], "brand_name": "Minocycline Hydrochloride", "product_id": "0591-5694_2d74faa2-99c4-4f01-adc6-60110d2b24da", "dosage_form": "CAPSULE", "pharm_class": ["Decreased Prothrombin Activity [PE]", "Tetracycline-class Drug [EPC]", "Tetracyclines [CS]"], "product_ndc": "0591-5694", "generic_name": "Minocycline Hydrochloride", "labeler_name": "Actavis Pharma, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Minocycline Hydrochloride", "active_ingredients": [{"name": "MINOCYCLINE HYDROCHLORIDE", "strength": "50 mg/1"}], "application_number": "ANDA063181", "marketing_category": "ANDA", "marketing_start_date": "19920201", "listing_expiration_date": "20261231"}