0591-3153
Generic: minocycline hydrochloride
Labeler: actavis pharma, inc.Drug Facts
Product Profile
Brand Name
Generic Name
minocycline hydrochloride
Labeler
actavis pharma, inc.
Dosage Form
CAPSULE
Active Ingredients
minocycline hydrochloride 75 mg/1
Identifiers & Regulatory
Product NDC
0591-3153
Product ID
0591-3153_f15795be-cc42-4d05-827e-715c25af1db7
Product Type
DRUG FOR FURTHER PROCESSING
Marketing Category
DRUG FOR FURTHER PROCESSING
Listing Expiration
2026-12-31
Marketing Start
1999-06-10
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
05913153
Hyphenated Format
0591-3153
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: label)
Generic Name
minocycline hydrochloride (source: ndc)
Application Number
ANDA063065 (source: label)
Routes
source: label
Resolved Composition
Strengths
- 75 mg/1
Packaging
- 39840 CAPSULE in 1 BOX (0591-3153-00)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"spl_id": "f15795be-cc42-4d05-827e-715c25af1db7", "openfda": {}, "finished": false, "packaging": [{"description": "39840 CAPSULE in 1 BOX (0591-3153-00)", "package_ndc": "0591-3153-00", "marketing_start_date": "10-JUN-99"}], "product_id": "0591-3153_f15795be-cc42-4d05-827e-715c25af1db7", "dosage_form": "CAPSULE", "product_ndc": "0591-3153", "generic_name": "Minocycline Hydrochloride", "labeler_name": "Actavis Pharma, Inc.", "product_type": "DRUG FOR FURTHER PROCESSING", "brand_name_base": null, "active_ingredients": [{"name": "MINOCYCLINE HYDROCHLORIDE", "strength": "75 mg/1"}], "marketing_category": "DRUG FOR FURTHER PROCESSING", "marketing_start_date": "19990610", "listing_expiration_date": "20261231"}