minocycline hydrochloride
Generic: minocycline hydrochloride
Labeler: pd-rx pharmaceuticals, inc.Drug Facts
Product Profile
Brand Name
minocycline hydrochloride
Generic Name
minocycline hydrochloride
Labeler
pd-rx pharmaceuticals, inc.
Dosage Form
CAPSULE
Routes
Active Ingredients
minocycline hydrochloride 50 mg/1
Manufacturer
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
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
55289202
Hyphenated Format
55289-202
Supplemental Identifiers
RxCUI
UPC
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
ANDA063181 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 50 mg/1
Packaging
- 30 CAPSULE in 1 BOTTLE, PLASTIC (55289-202-30)
Packages (1)
Ingredients (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"}