minocycline hydrochloride

Generic: minocycline hydrochloride

Labeler: chartwell rx, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name minocycline hydrochloride
Generic Name minocycline hydrochloride
Labeler chartwell rx, llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

minocycline hydrochloride 100 mg/1

Manufacturer
Chartwell RX, LLC

Identifiers & Regulatory

Product NDC 62135-889
Product ID 62135-889_37c8b548-71eb-bac3-e063-6394a90a7052
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA065436
Listing Expiration 2026-12-31
Marketing Start 2007-12-26

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 62135889
Hyphenated Format 62135-889

Supplemental Identifiers

RxCUI
207362 207364 403840
UPC
0362135888602 0362135887902 0362135889609
UNII
0020414E5U

Packaging Origin

Original Packager
true

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 ANDA065436 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 100 mg/1
source: ndc
Packaging
  • 60 TABLET in 1 BOTTLE (62135-889-60)
source: ndc

Packages (1)

62135-889-60 60 TABLET in 1 BOTTLE (62135-889-60)

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": "37c8b548-71eb-bac3-e063-6394a90a7052", "openfda": {"upc": ["0362135888602", "0362135887902", "0362135889609"], "unii": ["0020414E5U"], "rxcui": ["207362", "207364", "403840"], "spl_set_id": ["43fbe7ff-4b67-474d-bf27-e5710d8d10ac"], "manufacturer_name": ["Chartwell RX, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET in 1 BOTTLE (62135-889-60)", "package_ndc": "62135-889-60", "marketing_start_date": "20250613"}], "brand_name": "Minocycline Hydrochloride", "product_id": "62135-889_37c8b548-71eb-bac3-e063-6394a90a7052", "dosage_form": "TABLET", "pharm_class": ["Decreased Prothrombin Activity [PE]", "Tetracycline-class Drug [EPC]", "Tetracyclines [CS]"], "product_ndc": "62135-889", "generic_name": "Minocycline Hydrochloride", "labeler_name": "Chartwell RX, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Minocycline Hydrochloride", "active_ingredients": [{"name": "MINOCYCLINE HYDROCHLORIDE", "strength": "100 mg/1"}], "application_number": "ANDA065436", "marketing_category": "ANDA", "marketing_start_date": "20071226", "listing_expiration_date": "20261231"}