minocycline hydrochloride

Generic: minocycline hydrochloride

Labeler: sun pharmaceutical industries, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name minocycline hydrochloride
Generic Name minocycline hydrochloride
Labeler sun pharmaceutical industries, inc.
Dosage Form CAPSULE
Routes
ORAL
Active Ingredients

minocycline hydrochloride 75 mg/1

Manufacturer
Sun Pharmaceutical Industries, Inc.

Identifiers & Regulatory

Product NDC 57664-852
Product ID 57664-852_330a0641-aaa9-e9c1-e063-6294a90ada9e
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA090867
Listing Expiration 2026-12-31
Marketing Start 2013-05-13

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 57664852
Hyphenated Format 57664-852

Supplemental Identifiers

RxCUI
197984 197985 314108
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 ANDA090867 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 75 mg/1
source: ndc
Packaging
  • 500 CAPSULE in 1 BOTTLE (57664-852-13)
  • 100 CAPSULE in 1 BOTTLE (57664-852-88)
source: ndc

Packages (2)

57664-852-13 500 CAPSULE in 1 BOTTLE (57664-852-13) 57664-852-88 100 CAPSULE in 1 BOTTLE (57664-852-88)

Ingredients (1)

minocycline hydrochloride (75 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": "330a0641-aaa9-e9c1-e063-6294a90ada9e", "openfda": {"unii": ["0020414E5U"], "rxcui": ["197984", "197985", "314108"], "spl_set_id": ["ddd14292-3e39-4f2d-92f2-e7a6253f200a"], "manufacturer_name": ["Sun Pharmaceutical Industries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 CAPSULE in 1 BOTTLE (57664-852-13)", "package_ndc": "57664-852-13", "marketing_start_date": "20130513"}, {"sample": false, "description": "100 CAPSULE in 1 BOTTLE (57664-852-88)", "package_ndc": "57664-852-88", "marketing_start_date": "20130513"}], "brand_name": "Minocycline Hydrochloride", "product_id": "57664-852_330a0641-aaa9-e9c1-e063-6294a90ada9e", "dosage_form": "CAPSULE", "pharm_class": ["Decreased Prothrombin Activity [PE]", "Tetracycline-class Drug [EPC]", "Tetracyclines [CS]"], "product_ndc": "57664-852", "generic_name": "Minocycline Hydrochloride", "labeler_name": "Sun Pharmaceutical Industries, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Minocycline Hydrochloride", "active_ingredients": [{"name": "MINOCYCLINE HYDROCHLORIDE", "strength": "75 mg/1"}], "application_number": "ANDA090867", "marketing_category": "ANDA", "marketing_start_date": "20130513", "listing_expiration_date": "20261231"}