minocycline hydrochloride
Generic: minocycline hydrochloride
Labeler: ascend laboratories, llcDrug Facts
Product Profile
Brand Name
minocycline hydrochloride
Generic Name
minocycline hydrochloride
Labeler
ascend laboratories, llc
Dosage Form
TABLET, FILM COATED, EXTENDED RELEASE
Routes
Active Ingredients
minocycline hydrochloride 90 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
67877-576
Product ID
67877-576_51213aa1-873c-4b55-a36d-3ebbb73fa220
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA204453
Listing Expiration
2026-12-31
Marketing Start
2016-09-30
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
67877576
Hyphenated Format
67877-576
Supplemental Identifiers
RxCUI
UNII
Packaging Origin
Original Packager
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
ANDA204453 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 90 mg/1
Packaging
- 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (67877-576-01)
- 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (67877-576-05)
- 10 BLISTER PACK in 1 CARTON (67877-576-14) / 14 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK
- 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (67877-576-30)
Packages (4)
67877-576-01
100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (67877-576-01)
67877-576-05
500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (67877-576-05)
67877-576-14
10 BLISTER PACK in 1 CARTON (67877-576-14) / 14 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK
67877-576-30
30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (67877-576-30)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "51213aa1-873c-4b55-a36d-3ebbb73fa220", "openfda": {"unii": ["0020414E5U"], "rxcui": ["629695", "629697", "629699", "858062", "858372", "1013659", "1013662", "1013665"], "spl_set_id": ["a8f95207-b259-4f50-87f2-3652d9268890"], "manufacturer_name": ["Ascend Laboratories, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (67877-576-01)", "package_ndc": "67877-576-01", "marketing_start_date": "20160930"}, {"sample": false, "description": "500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (67877-576-05)", "package_ndc": "67877-576-05", "marketing_start_date": "20160930"}, {"sample": false, "description": "10 BLISTER PACK in 1 CARTON (67877-576-14) / 14 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK", "package_ndc": "67877-576-14", "marketing_start_date": "20160930"}, {"sample": false, "description": "30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (67877-576-30)", "package_ndc": "67877-576-30", "marketing_start_date": "20160930"}], "brand_name": "Minocycline Hydrochloride", "product_id": "67877-576_51213aa1-873c-4b55-a36d-3ebbb73fa220", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "pharm_class": ["Decreased Prothrombin Activity [PE]", "Tetracycline-class Drug [EPC]", "Tetracyclines [CS]"], "product_ndc": "67877-576", "generic_name": "Minocycline Hydrochloride", "labeler_name": "Ascend Laboratories, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Minocycline Hydrochloride", "active_ingredients": [{"name": "MINOCYCLINE HYDROCHLORIDE", "strength": "90 mg/1"}], "application_number": "ANDA204453", "marketing_category": "ANDA", "marketing_start_date": "20160930", "listing_expiration_date": "20261231"}