minocycline hydrochloride

Generic: minocycline hydrochloride

Labeler: pd-rx pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name minocycline hydrochloride
Generic Name minocycline hydrochloride
Labeler pd-rx pharmaceuticals, inc.
Dosage Form CAPSULE
Routes
ORAL
Active Ingredients

minocycline hydrochloride 50 mg/1

Manufacturer
PD-Rx Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 55289-202
Product ID 55289-202_2abe4929-7b43-f97c-e063-6294a90a198c
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 55289202
Hyphenated Format 55289-202

Supplemental Identifiers

RxCUI
197985
UPC
0355289202301
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 ANDA063181 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 50 mg/1
source: ndc
Packaging
  • 30 CAPSULE in 1 BOTTLE, PLASTIC (55289-202-30)
source: ndc

Packages (1)

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": "2abe4929-7b43-f97c-e063-6294a90a198c", "openfda": {"upc": ["0355289202301"], "unii": ["0020414E5U"], "rxcui": ["197985"], "spl_set_id": ["1ec20539-0421-4eac-95ed-e9acc6329fd0"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE in 1 BOTTLE, PLASTIC (55289-202-30)", "package_ndc": "55289-202-30", "marketing_start_date": "20110830"}], "brand_name": "Minocycline Hydrochloride", "product_id": "55289-202_2abe4929-7b43-f97c-e063-6294a90a198c", "dosage_form": "CAPSULE", "pharm_class": ["Decreased Prothrombin Activity [PE]", "Tetracycline-class Drug [EPC]", "Tetracyclines [CS]"], "product_ndc": "55289-202", "generic_name": "Minocycline Hydrochloride", "labeler_name": "PD-Rx Pharmaceuticals, 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"}