minocycline hydrochloride

Generic: minocycline hydrochloride

Labeler: a-s medication solutions
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name minocycline hydrochloride
Generic Name minocycline hydrochloride
Labeler a-s medication solutions
Dosage Form CAPSULE
Routes
ORAL
Active Ingredients

minocycline hydrochloride 100 mg/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-2339
Product ID 50090-2339_d8f6f6f4-678b-4e0e-984d-1a10498453af
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA065062
Listing Expiration 2026-12-31
Marketing Start 2015-04-02

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 500902339
Hyphenated Format 50090-2339

Supplemental Identifiers

RxCUI
197984
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 ANDA065062 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 100 mg/1
source: ndc
Packaging
  • 60 CAPSULE in 1 BOTTLE (50090-2339-0)
  • 20 CAPSULE in 1 BOTTLE (50090-2339-2)
  • 30 CAPSULE in 1 BOTTLE (50090-2339-3)
  • 90 CAPSULE in 1 BOTTLE (50090-2339-4)
source: ndc

Packages (4)

50090-2339-0 60 CAPSULE in 1 BOTTLE (50090-2339-0) 50090-2339-2 20 CAPSULE in 1 BOTTLE (50090-2339-2) 50090-2339-3 30 CAPSULE in 1 BOTTLE (50090-2339-3) 50090-2339-4 90 CAPSULE in 1 BOTTLE (50090-2339-4)

Ingredients (1)

minocycline hydrochloride (100 mg/1)

Linked Drug Pages (1)

Minocycline Hydrochloride ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "d8f6f6f4-678b-4e0e-984d-1a10498453af", "openfda": {"unii": ["0020414E5U"], "rxcui": ["197984"], "spl_set_id": ["c7d0226e-5ac5-4fb1-9849-9d6663a2e8ad"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "60 CAPSULE in 1 BOTTLE (50090-2339-0)", "package_ndc": "50090-2339-0", "marketing_start_date": "20160404"}, {"sample": false, "description": "20 CAPSULE in 1 BOTTLE (50090-2339-2)", "package_ndc": "50090-2339-2", "marketing_start_date": "20160404"}, {"sample": false, "description": "30 CAPSULE in 1 BOTTLE (50090-2339-3)", "package_ndc": "50090-2339-3", "marketing_start_date": "20160404"}, {"sample": false, "description": "90 CAPSULE in 1 BOTTLE (50090-2339-4)", "package_ndc": "50090-2339-4", "marketing_start_date": "20160404"}], "brand_name": "Minocycline Hydrochloride", "product_id": "50090-2339_d8f6f6f4-678b-4e0e-984d-1a10498453af", "dosage_form": "CAPSULE", "pharm_class": ["Decreased Prothrombin Activity [PE]", "Tetracycline-class Drug [EPC]", "Tetracyclines [CS]"], "product_ndc": "50090-2339", "generic_name": "Minocycline Hydrochloride", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Minocycline Hydrochloride", "active_ingredients": [{"name": "MINOCYCLINE HYDROCHLORIDE", "strength": "100 mg/1"}], "application_number": "ANDA065062", "marketing_category": "ANDA", "marketing_start_date": "20150402", "listing_expiration_date": "20261231"}