hydromorphone hydrochloride

Generic: hydromorphone hydrochloride

Labeler: american health packaging
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name hydromorphone hydrochloride
Generic Name hydromorphone hydrochloride
Labeler american health packaging
Dosage Form TABLET
Routes
ORAL
Active Ingredients

hydromorphone hydrochloride 2 mg/1

Manufacturer
American Health Packaging

Identifiers & Regulatory

Product NDC 60687-579
Product ID 60687-579_4bd4edc0-b58e-cd45-e063-6294a90a779c
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA076855
DEA Schedule cii
Listing Expiration 2027-12-31
Marketing Start 2021-05-11

Pharmacologic Class

Classes
full opioid agonists [moa] opioid agonist [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 60687579
Hyphenated Format 60687-579

Supplemental Identifiers

RxCUI
897696 897702
UNII
L960UP2KRW

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 hydromorphone hydrochloride (source: ndc)
Generic Name hydromorphone hydrochloride (source: ndc)
Application Number ANDA076855 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 2 mg/1
source: ndc
Packaging
  • 100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-579-01) / 1 TABLET in 1 BLISTER PACK (60687-579-11)
source: ndc

Packages (1)

60687-579-01 100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-579-01) / 1 TABLET in 1 BLISTER PACK (60687-579-11)

Ingredients (1)

hydromorphone hydrochloride (2 mg/1)

Linked Drug Pages (1)

Hydromorphone Hydrochloride ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "4bd4edc0-b58e-cd45-e063-6294a90a779c", "openfda": {"unii": ["L960UP2KRW"], "rxcui": ["897696", "897702"], "spl_set_id": ["e4758743-9b2c-4612-8399-ad2db372e2b7"], "manufacturer_name": ["American Health Packaging"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-579-01)  / 1 TABLET in 1 BLISTER PACK (60687-579-11)", "package_ndc": "60687-579-01", "marketing_start_date": "20210511"}], "brand_name": "Hydromorphone Hydrochloride", "product_id": "60687-579_4bd4edc0-b58e-cd45-e063-6294a90a779c", "dosage_form": "TABLET", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "60687-579", "dea_schedule": "CII", "generic_name": "Hydromorphone Hydrochloride", "labeler_name": "American Health Packaging", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Hydromorphone Hydrochloride", "active_ingredients": [{"name": "HYDROMORPHONE HYDROCHLORIDE", "strength": "2 mg/1"}], "application_number": "ANDA076855", "marketing_category": "ANDA", "marketing_start_date": "20210511", "listing_expiration_date": "20271231"}