minocycline hydrochloride

Generic: minocycline hydrochloride

Labeler: proficient rx lp
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name minocycline hydrochloride
Generic Name minocycline hydrochloride
Labeler proficient rx lp
Dosage Form CAPSULE
Routes
ORAL
Active Ingredients

minocycline hydrochloride 100 mg/1

Manufacturer
Proficient Rx LP

Identifiers & Regulatory

Product NDC 71205-272
Product ID 71205-272_716c5abe-6d0e-4cfd-9c37-45a967e136ec
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA065470
Listing Expiration 2026-12-31
Marketing Start 2008-03-11

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 71205272
Hyphenated Format 71205-272

Supplemental Identifiers

RxCUI
197984
UPC
0371205272210
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
  • 20 CAPSULE in 1 BOTTLE (71205-272-20)
  • 21 CAPSULE in 1 BOTTLE (71205-272-21)
  • 30 CAPSULE in 1 BOTTLE (71205-272-30)
  • 60 CAPSULE in 1 BOTTLE (71205-272-60)
  • 90 CAPSULE in 1 BOTTLE (71205-272-90)
source: ndc

Packages (5)

71205-272-20 20 CAPSULE in 1 BOTTLE (71205-272-20) 71205-272-21 21 CAPSULE in 1 BOTTLE (71205-272-21) 71205-272-30 30 CAPSULE in 1 BOTTLE (71205-272-30) 71205-272-60 60 CAPSULE in 1 BOTTLE (71205-272-60) 71205-272-90 90 CAPSULE in 1 BOTTLE (71205-272-90)

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": "716c5abe-6d0e-4cfd-9c37-45a967e136ec", "openfda": {"upc": ["0371205272210"], "unii": ["0020414E5U"], "rxcui": ["197984"], "spl_set_id": ["4f904969-5af3-461e-b557-d03a1e5c7292"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "20 CAPSULE in 1 BOTTLE (71205-272-20)", "package_ndc": "71205-272-20", "marketing_start_date": "20190501"}, {"sample": false, "description": "21 CAPSULE in 1 BOTTLE (71205-272-21)", "package_ndc": "71205-272-21", "marketing_start_date": "20190501"}, {"sample": false, "description": "30 CAPSULE in 1 BOTTLE (71205-272-30)", "package_ndc": "71205-272-30", "marketing_start_date": "20190501"}, {"sample": false, "description": "60 CAPSULE in 1 BOTTLE (71205-272-60)", "package_ndc": "71205-272-60", "marketing_start_date": "20190501"}, {"sample": false, "description": "90 CAPSULE in 1 BOTTLE (71205-272-90)", "package_ndc": "71205-272-90", "marketing_start_date": "20190501"}], "brand_name": "Minocycline Hydrochloride", "product_id": "71205-272_716c5abe-6d0e-4cfd-9c37-45a967e136ec", "dosage_form": "CAPSULE", "pharm_class": ["Decreased Prothrombin Activity [PE]", "Tetracycline-class Drug [EPC]", "Tetracyclines [CS]"], "product_ndc": "71205-272", "generic_name": "Minocycline Hydrochloride", "labeler_name": "Proficient Rx LP", "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": "20080311", "listing_expiration_date": "20261231"}