minocycline hydrochloride

Generic: minocycline hydrochloride

Labeler: bryant ranch prepack
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name minocycline hydrochloride
Generic Name minocycline hydrochloride
Labeler bryant ranch prepack
Dosage Form TABLET, FILM COATED, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

minocycline hydrochloride 135 mg/1

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 72162-1853
Product ID 72162-1853_2679876a-7c6d-49cc-bf96-732394bb1013
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA204453
Listing Expiration 2026-12-31
Marketing Start 2016-09-30

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 721621853
Hyphenated Format 72162-1853

Supplemental Identifiers

RxCUI
629695
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 ANDA204453 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 135 mg/1
source: ndc
Packaging
  • 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72162-1853-3)
source: ndc

Packages (1)

72162-1853-3 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72162-1853-3)

Ingredients (1)

minocycline hydrochloride (135 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": "2679876a-7c6d-49cc-bf96-732394bb1013", "openfda": {"unii": ["0020414E5U"], "rxcui": ["629695"], "spl_set_id": ["409dddb0-be3a-4ae3-ab39-88a6cd50a219"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72162-1853-3)", "package_ndc": "72162-1853-3", "marketing_start_date": "20240311"}], "brand_name": "Minocycline Hydrochloride", "product_id": "72162-1853_2679876a-7c6d-49cc-bf96-732394bb1013", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "pharm_class": ["Decreased Prothrombin Activity [PE]", "Tetracycline-class Drug [EPC]", "Tetracyclines [CS]"], "product_ndc": "72162-1853", "generic_name": "Minocycline Hydrochloride", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Minocycline Hydrochloride", "active_ingredients": [{"name": "MINOCYCLINE HYDROCHLORIDE", "strength": "135 mg/1"}], "application_number": "ANDA204453", "marketing_category": "ANDA", "marketing_start_date": "20160930", "listing_expiration_date": "20261231"}