minocycline hydrochloride
Generic: minocycline hydrochloride
Labeler: major pharamceuticalsDrug Facts
Product Profile
Brand Name
minocycline hydrochloride
Generic Name
minocycline hydrochloride
Labeler
major pharamceuticals
Dosage Form
CAPSULE
Routes
Active Ingredients
minocycline hydrochloride 100 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
0904-6888
Product ID
0904-6888_aed0618f-2e64-4e18-991b-1e38efcf56b2
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA065062
Listing Expiration
2026-12-31
Marketing Start
2015-04-02
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
09046888
Hyphenated Format
0904-6888
Supplemental Identifiers
RxCUI
UNII
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
ANDA065062 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 100 mg/1
Packaging
- 50 BLISTER PACK in 1 CARTON (0904-6888-06) / 1 CAPSULE in 1 BLISTER PACK
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "aed0618f-2e64-4e18-991b-1e38efcf56b2", "openfda": {"unii": ["0020414E5U"], "rxcui": ["197984"], "spl_set_id": ["fd86ff45-37d0-4501-b9fb-e1836e4a8be4"], "manufacturer_name": ["Major Pharamceuticals"]}, "finished": true, "packaging": [{"sample": false, "description": "50 BLISTER PACK in 1 CARTON (0904-6888-06) / 1 CAPSULE in 1 BLISTER PACK", "package_ndc": "0904-6888-06", "marketing_start_date": "20150402"}], "brand_name": "Minocycline Hydrochloride", "product_id": "0904-6888_aed0618f-2e64-4e18-991b-1e38efcf56b2", "dosage_form": "CAPSULE", "pharm_class": ["Decreased Prothrombin Activity [PE]", "Tetracycline-class Drug [EPC]", "Tetracyclines [CS]"], "product_ndc": "0904-6888", "generic_name": "Minocycline Hydrochloride", "labeler_name": "Major Pharamceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Minocycline Hydrochloride", "active_ingredients": [{"name": "MINOCYCLINE HYDROCHLORIDE", "strength": "100 mg/1"}], "application_number": "ANDA065062", "marketing_category": "ANDA", "marketing_start_date": "20150402", "listing_expiration_date": "20261231"}