tadalafil

Generic: tadalafil

Labeler: camber pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name tadalafil
Generic Name tadalafil
Labeler camber pharmaceuticals, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

tadalafil 20 mg/1

Manufacturer
Camber Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 31722-647
Product ID 31722-647_0b3039c8-da1b-416b-e063-6294a90ae7c2
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA209907
Listing Expiration 2026-12-31
Marketing Start 2019-02-05

Pharmacologic Class

Established (EPC)
phosphodiesterase 5 inhibitor [epc]
Mechanism of Action
phosphodiesterase 5 inhibitors [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 31722647
Hyphenated Format 31722-647

Supplemental Identifiers

RxCUI
2123194
UPC
0331722647311 0331722647304
UNII
742SXX0ICT
NUI
N0000175599 N0000020026

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 tadalafil (source: ndc)
Generic Name tadalafil (source: ndc)
Application Number ANDA209907 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (31722-647-30)
  • 10 BLISTER PACK in 1 CARTON (31722-647-31) / 10 TABLET in 1 BLISTER PACK
  • 60 TABLET in 1 BOTTLE (31722-647-60)
source: ndc

Packages (3)

31722-647-30 30 TABLET in 1 BOTTLE (31722-647-30) 31722-647-31 10 BLISTER PACK in 1 CARTON (31722-647-31) / 10 TABLET in 1 BLISTER PACK 31722-647-60 60 TABLET in 1 BOTTLE (31722-647-60)

Ingredients (1)

tadalafil (20 mg/1)

Linked Drug Pages (1)

Tadalafil ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "0b3039c8-da1b-416b-e063-6294a90ae7c2", "openfda": {"nui": ["N0000175599", "N0000020026"], "upc": ["0331722647311", "0331722647304"], "unii": ["742SXX0ICT"], "rxcui": ["2123194"], "spl_set_id": ["dc0a6a03-5ef1-4507-b888-5b559653c3e9"], "pharm_class_epc": ["Phosphodiesterase 5 Inhibitor [EPC]"], "pharm_class_moa": ["Phosphodiesterase 5 Inhibitors [MoA]"], "manufacturer_name": ["Camber Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (31722-647-30)", "package_ndc": "31722-647-30", "marketing_start_date": "20190205"}, {"sample": false, "description": "10 BLISTER PACK in 1 CARTON (31722-647-31)  / 10 TABLET in 1 BLISTER PACK", "package_ndc": "31722-647-31", "marketing_start_date": "20190205"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (31722-647-60)", "package_ndc": "31722-647-60", "marketing_start_date": "20200330"}], "brand_name": "Tadalafil", "product_id": "31722-647_0b3039c8-da1b-416b-e063-6294a90ae7c2", "dosage_form": "TABLET", "pharm_class": ["Phosphodiesterase 5 Inhibitor [EPC]", "Phosphodiesterase 5 Inhibitors [MoA]"], "product_ndc": "31722-647", "generic_name": "Tadalafil", "labeler_name": "Camber Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Tadalafil", "active_ingredients": [{"name": "TADALAFIL", "strength": "20 mg/1"}], "application_number": "ANDA209907", "marketing_category": "ANDA", "marketing_start_date": "20190205", "listing_expiration_date": "20261231"}