DRONABINOL

Generic: DRONABINOL

Labeler: American Health Packaging
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive

Drug Facts

Product Profile

Brand Name DRONABINOL
Generic Name DRONABINOL
Labeler American Health Packaging
Dosage Form CAPSULE
Routes
ORAL
Active Ingredients

DRONABINOL 5 mg/1

Identifiers & Regulatory

Product NDC 60687-386
Product ID 60687-386_2b22b30c-d0ac-1724-e063-6294a90af085
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA078292
DEA Schedule CIII
Marketing Start 2018-10-02
Marketing End 2026-02-28

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 60687386
Hyphenated Format 60687-386

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 DRONABINOL (source: ndc)
Generic Name DRONABINOL (source: ndc)
Application Number ANDA078292 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 5 mg/1
source: ndc
Packaging
  • 20 BLISTER PACK in 1 CARTON (60687-386-94) / 1 CAPSULE in 1 BLISTER PACK (60687-386-11)
source: ndc

Packages (1)

Ingredients (1)

DRONABINOL (5 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2b22b30c-d0ac-1724-e063-6294a90af085", "openfda": {"nui": ["N0000175782", "M0003267"], "unii": ["7J8897W37S"], "rxcui": ["197635", "197636"], "spl_set_id": ["35e04467-d429-4fe8-a7d8-b9d8f8376b5b"], "pharm_class_cs": ["Cannabinoids [CS]"], "pharm_class_epc": ["Cannabinoid [EPC]"], "manufacturer_name": ["American Health Packaging"]}, "finished": true, "packaging": [{"sample": false, "description": "20 BLISTER PACK in 1 CARTON (60687-386-94)  / 1 CAPSULE in 1 BLISTER PACK (60687-386-11)", "package_ndc": "60687-386-94", "marketing_end_date": "20260228", "marketing_start_date": "20240508"}], "brand_name": "DRONABINOL", "product_id": "60687-386_2b22b30c-d0ac-1724-e063-6294a90af085", "dosage_form": "CAPSULE", "pharm_class": ["Cannabinoid [EPC]", "Cannabinoids [CS]"], "product_ndc": "60687-386", "dea_schedule": "CIII", "generic_name": "DRONABINOL", "labeler_name": "American Health Packaging", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "DRONABINOL", "active_ingredients": [{"name": "DRONABINOL", "strength": "5 mg/1"}], "application_number": "ANDA078292", "marketing_category": "ANDA", "marketing_end_date": "20260228", "marketing_start_date": "20181002"}