carbidopa

Generic: carbidopa

Labeler: northstar rx llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name carbidopa
Generic Name carbidopa
Labeler northstar rx llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

carbidopa 25 mg/1

Manufacturer
NorthStar Rx LLC

Identifiers & Regulatory

Product NDC 16714-067
Product ID 16714-067_65000b5a-3d2e-4228-8757-cca85e663c80
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA211055
Listing Expiration 2026-12-31
Marketing Start 2019-10-21

Pharmacologic Class

Established (EPC)
aromatic amino acid decarboxylation inhibitor [epc]
Mechanism of Action
dopa decarboxylase inhibitors [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 16714067
Hyphenated Format 16714-067

Supplemental Identifiers

RxCUI
260260
UNII
MNX7R8C5VO
NUI
N0000175754 N0000175755

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 carbidopa (source: ndc)
Generic Name carbidopa (source: ndc)
Application Number ANDA211055 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 25 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (16714-067-01)
source: ndc

Packages (1)

Ingredients (1)

carbidopa (25 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "65000b5a-3d2e-4228-8757-cca85e663c80", "openfda": {"nui": ["N0000175754", "N0000175755"], "unii": ["MNX7R8C5VO"], "rxcui": ["260260"], "spl_set_id": ["33ee4598-cbcc-45e0-a48e-dc0101e1f204"], "pharm_class_epc": ["Aromatic Amino Acid Decarboxylation Inhibitor [EPC]"], "pharm_class_moa": ["DOPA Decarboxylase Inhibitors [MoA]"], "manufacturer_name": ["NorthStar Rx LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (16714-067-01)", "package_ndc": "16714-067-01", "marketing_start_date": "20191021"}], "brand_name": "Carbidopa", "product_id": "16714-067_65000b5a-3d2e-4228-8757-cca85e663c80", "dosage_form": "TABLET", "product_ndc": "16714-067", "generic_name": "Carbidopa", "labeler_name": "NorthStar Rx LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Carbidopa", "active_ingredients": [{"name": "CARBIDOPA", "strength": "25 mg/1"}], "application_number": "ANDA211055", "marketing_category": "ANDA", "marketing_start_date": "20191021", "listing_expiration_date": "20261231"}