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 50 mg/1

Manufacturer
Proficient Rx LP

Identifiers & Regulatory

Product NDC 71205-086
Product ID 71205-086_a2baa928-f954-40a1-a0e7-f7e373f5d3eb
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA063181
Listing Expiration 2026-12-31
Marketing Start 1992-02-01

Pharmacologic Class

Classes
tetracycline-class drug [epc] tetracyclines [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 71205086
Hyphenated Format 71205-086

Supplemental Identifiers

RxCUI
197985
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 ANDA063181 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 50 mg/1
source: ndc
Packaging
  • 20 CAPSULE in 1 BOTTLE, PLASTIC (71205-086-20)
  • 21 CAPSULE in 1 BOTTLE, PLASTIC (71205-086-21)
  • 30 CAPSULE in 1 BOTTLE, PLASTIC (71205-086-30)
  • 60 CAPSULE in 1 BOTTLE, PLASTIC (71205-086-60)
  • 90 CAPSULE in 1 BOTTLE, PLASTIC (71205-086-90)
source: ndc

Packages (5)

Ingredients (1)

minocycline hydrochloride (50 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "a2baa928-f954-40a1-a0e7-f7e373f5d3eb", "openfda": {"unii": ["0020414E5U"], "rxcui": ["197985"], "spl_set_id": ["d5fcba91-6aa6-4072-aea5-fb8da65d9aac"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "20 CAPSULE in 1 BOTTLE, PLASTIC (71205-086-20)", "package_ndc": "71205-086-20", "marketing_start_date": "20180801"}, {"sample": false, "description": "21 CAPSULE in 1 BOTTLE, PLASTIC (71205-086-21)", "package_ndc": "71205-086-21", "marketing_start_date": "20180801"}, {"sample": false, "description": "30 CAPSULE in 1 BOTTLE, PLASTIC (71205-086-30)", "package_ndc": "71205-086-30", "marketing_start_date": "20180801"}, {"sample": false, "description": "60 CAPSULE in 1 BOTTLE, PLASTIC (71205-086-60)", "package_ndc": "71205-086-60", "marketing_start_date": "20180801"}, {"sample": false, "description": "90 CAPSULE in 1 BOTTLE, PLASTIC (71205-086-90)", "package_ndc": "71205-086-90", "marketing_start_date": "20220103"}], "brand_name": "Minocycline Hydrochloride", "product_id": "71205-086_a2baa928-f954-40a1-a0e7-f7e373f5d3eb", "dosage_form": "CAPSULE", "pharm_class": ["Tetracycline-class Drug [EPC]", "Tetracyclines [CS]"], "product_ndc": "71205-086", "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": "50 mg/1"}], "application_number": "ANDA063181", "marketing_category": "ANDA", "marketing_start_date": "19920201", "listing_expiration_date": "20261231"}