Luffa - 60986-2025-2 - (Luffa, Hydrastis Canadensis, Mercurius Sulph. Rub, Allium Cepa, Natrum Muriticum, Phosphorus, Eupatorium Perf, Sticta)

Alphabetical Index


Drug Information of Luffa

Product NDC: 60986-2025
Proprietary Name: Luffa
Non Proprietary Name: Luffa, Hydrastis Canadensis, Mercurius Sulph. Rub, Allium Cepa, Natrum Muriticum, Phosphorus, Eupatorium Perf, Sticta
Active Ingredient(s): 5; 4; 2; 6; 4; 6; 6; 6    [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1 & nbsp;   Luffa, Hydrastis Canadensis, Mercurius Sulph. Rub, Allium Cepa, Natrum Muriticum, Phosphorus, Eupatorium Perf, Sticta
Administration Route(s): ORAL
Dosage Form(s): TABLET, ORALLY DISINTEGRATING
Coding System: National Drug Codes(NDC)

Labeler Information of Luffa

Product NDC: 60986-2025
Labeler Name: Marco Pharma International LLC.
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date: 19920301

Package Information of Luffa

Package NDC: 60986-2025-2
Package Description: 60 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE, PLASTIC (60986-2025-2)

NDC Information of Luffa

NDC Code 60986-2025-2
Proprietary Name Luffa
Package Description 60 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE, PLASTIC (60986-2025-2)
Product NDC 60986-2025
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Luffa, Hydrastis Canadensis, Mercurius Sulph. Rub, Allium Cepa, Natrum Muriticum, Phosphorus, Eupatorium Perf, Sticta
Dosage Form Name TABLET, ORALLY DISINTEGRATING
Route Name ORAL
Start Marketing Date 19920301
Marketing Category Name UNAPPROVED HOMEOPATHIC
Labeler Name Marco Pharma International LLC.
Substance Name EUPATORIUM PERFOLIATUM FLOWERING TOP; GOLDENSEAL; LOBARIA PULMONARIA; LUFFA ACUTANGULA FRUIT; MERCURIC SULFIDE; ONION; PHOSPHORUS; SODIUM CHLORIDE
Strength Number 5; 4; 2; 6; 4; 6; 6; 6
Strength Unit [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1
Pharmaceutical Classes

Complete Information of Luffa


General Information