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 100 mg/1

Manufacturer
PD-Rx Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 43063-736
Product ID 43063-736_39fa09f2-a5b1-e1a4-e063-6394a90a173d
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 43063736
Hyphenated Format 43063-736

Supplemental Identifiers

RxCUI
197984
UPC
0343063736302
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
  • 14 CAPSULE in 1 BOTTLE, PLASTIC (43063-736-14)
  • 20 CAPSULE in 1 BOTTLE, PLASTIC (43063-736-20)
  • 30 CAPSULE in 1 BOTTLE, PLASTIC (43063-736-30)
  • 60 CAPSULE in 1 BOTTLE, PLASTIC (43063-736-60)
source: ndc

Packages (4)

43063-736-14 14 CAPSULE in 1 BOTTLE, PLASTIC (43063-736-14) 43063-736-20 20 CAPSULE in 1 BOTTLE, PLASTIC (43063-736-20) 43063-736-30 30 CAPSULE in 1 BOTTLE, PLASTIC (43063-736-30) 43063-736-60 60 CAPSULE in 1 BOTTLE, PLASTIC (43063-736-60)

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": "39fa09f2-a5b1-e1a4-e063-6394a90a173d", "openfda": {"upc": ["0343063736302"], "unii": ["0020414E5U"], "rxcui": ["197984"], "spl_set_id": ["7e2390b7-242c-43ff-afb3-b0a5e79351d3"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "14 CAPSULE in 1 BOTTLE, PLASTIC (43063-736-14)", "package_ndc": "43063-736-14", "marketing_start_date": "20170404"}, {"sample": false, "description": "20 CAPSULE in 1 BOTTLE, PLASTIC (43063-736-20)", "package_ndc": "43063-736-20", "marketing_start_date": "20170123"}, {"sample": false, "description": "30 CAPSULE in 1 BOTTLE, PLASTIC (43063-736-30)", "package_ndc": "43063-736-30", "marketing_start_date": "20170203"}, {"sample": false, "description": "60 CAPSULE in 1 BOTTLE, PLASTIC (43063-736-60)", "package_ndc": "43063-736-60", "marketing_start_date": "20170203"}], "brand_name": "Minocycline Hydrochloride", "product_id": "43063-736_39fa09f2-a5b1-e1a4-e063-6394a90a173d", "dosage_form": "CAPSULE", "pharm_class": ["Decreased Prothrombin Activity [PE]", "Tetracycline-class Drug [EPC]", "Tetracyclines [CS]"], "product_ndc": "43063-736", "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": "100 mg/1"}], "application_number": "ANDA065062", "marketing_category": "ANDA", "marketing_start_date": "20150402", "listing_expiration_date": "20261231"}