methyldopa

Generic: methyldopa

Labeler: rising pharma holdings, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name methyldopa
Generic Name methyldopa
Labeler rising pharma holdings, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

methyldopa 500 mg/1

Manufacturer
Rising Pharma Holdings, Inc.

Identifiers & Regulatory

Product NDC 64980-572
Product ID 64980-572_807ace4b-b2af-44b4-9371-884d73e21601
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA070076
Listing Expiration 2026-12-31
Marketing Start 2024-09-16

Pharmacologic Class

Classes
adrenergic alpha2-agonists [moa] central alpha-2 adrenergic agonist [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 64980572
Hyphenated Format 64980-572

Supplemental Identifiers

RxCUI
197956 197958
UNII
56LH93261Y

Packaging Origin

Original Packager
true

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 methyldopa (source: ndc)
Generic Name methyldopa (source: ndc)
Application Number ANDA070076 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 500 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (64980-572-01)
source: ndc

Packages (1)

Ingredients (1)

methyldopa (500 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "807ace4b-b2af-44b4-9371-884d73e21601", "openfda": {"unii": ["56LH93261Y"], "rxcui": ["197956", "197958"], "spl_set_id": ["9e22e1d8-04ec-4b67-92ea-b09c706f2703"], "manufacturer_name": ["Rising Pharma Holdings, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (64980-572-01)", "package_ndc": "64980-572-01", "marketing_start_date": "20240916"}], "brand_name": "Methyldopa", "product_id": "64980-572_807ace4b-b2af-44b4-9371-884d73e21601", "dosage_form": "TABLET", "pharm_class": ["Adrenergic alpha2-Agonists [MoA]", "Central alpha-2 Adrenergic Agonist [EPC]"], "product_ndc": "64980-572", "generic_name": "methyldopa", "labeler_name": "Rising Pharma Holdings, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Methyldopa", "active_ingredients": [{"name": "METHYLDOPA", "strength": "500 mg/1"}], "application_number": "ANDA070076", "marketing_category": "ANDA", "marketing_start_date": "20240916", "listing_expiration_date": "20261231"}