minocycline hydrochloride

Generic: minocycline hydrochloride

Labeler: remedyrepack inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name minocycline hydrochloride
Generic Name minocycline hydrochloride
Labeler remedyrepack inc.
Dosage Form CAPSULE
Routes
ORAL
Active Ingredients

minocycline hydrochloride 100 mg/1

Manufacturer
REMEDYREPACK INC.

Identifiers & Regulatory

Product NDC 70518-1336
Product ID 70518-1336_48d74037-829a-f6bc-e063-6294a90a7d50
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA065470
Listing Expiration 2027-12-31
Marketing Start 2018-08-01

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 705181336
Hyphenated Format 70518-1336

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 ANDA065470 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 100 mg/1
source: ndc
Packaging
  • 30 CAPSULE in 1 BLISTER PACK (70518-1336-1)
source: ndc

Packages (1)

70518-1336-1 30 CAPSULE in 1 BLISTER PACK (70518-1336-1)

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": "48d74037-829a-f6bc-e063-6294a90a7d50", "openfda": {"unii": ["0020414E5U"], "rxcui": ["197984"], "spl_set_id": ["0becbde8-6ec5-4830-a0d9-cfdb7b15eb84"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE in 1 BLISTER PACK (70518-1336-1)", "package_ndc": "70518-1336-1", "marketing_start_date": "20180821"}], "brand_name": "Minocycline Hydrochloride", "product_id": "70518-1336_48d74037-829a-f6bc-e063-6294a90a7d50", "dosage_form": "CAPSULE", "pharm_class": ["Decreased Prothrombin Activity [PE]", "Tetracycline-class Drug [EPC]", "Tetracyclines [CS]"], "product_ndc": "70518-1336", "generic_name": "Minocycline Hydrochloride", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Minocycline Hydrochloride", "active_ingredients": [{"name": "MINOCYCLINE HYDROCHLORIDE", "strength": "100 mg/1"}], "application_number": "ANDA065470", "marketing_category": "ANDA", "marketing_start_date": "20180801", "listing_expiration_date": "20271231"}