minocycline hydrochloride

Generic: minocycline hydrochloride

Labeler: actavis pharma, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name minocycline hydrochloride
Generic Name minocycline hydrochloride
Labeler actavis pharma, inc.
Dosage Form CAPSULE
Routes
ORAL
Active Ingredients

minocycline hydrochloride 50 mg/1

Manufacturer
Actavis Pharma, Inc.

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
decreased prothrombin activity [pe] tetracycline-class drug [epc] tetracyclines [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 05915694
Hyphenated Format 0591-5694

Supplemental Identifiers

RxCUI
197984 197985 314108
UPC
0305915694017
UNII
0020414E5U

Packaging Origin

Original Packager
true

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
ORAL
source: ndc

Resolved Composition

Strengths
  • 50 mg/1
source: ndc
Packaging
  • 100 CAPSULE in 1 BOTTLE, PLASTIC (0591-5694-01)
  • 60 CAPSULE in 1 BOTTLE, PLASTIC (0591-5694-60)
source: ndc

Packages (2)

Ingredients (1)

minocycline hydrochloride (50 mg/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"}