NDC 15631-0261

LACHESIS MUTUS

Lachesis Mutus

LACHESIS MUTUS is a Oral Pellet in the Human Otc Drug category. It is labeled and distributed by Rxhomeo Private Limited D.b.a. Rxhomeo, Inc. The primary component is Lachesis Muta Venom.

Product ID15631-0261_4d3d79ea-b865-4a96-9fcb-2c50caebf59e
NDC15631-0261
Product TypeHuman Otc Drug
Proprietary NameLACHESIS MUTUS
Generic NameLachesis Mutus
Dosage FormPellet
Route of AdministrationORAL
Marketing Start Date2015-09-05
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameRxhomeo Private Limited d.b.a. Rxhomeo, Inc
Substance NameLACHESIS MUTA VENOM
Active Ingredient Strength8 [hp_X]/1
NDC Exclude FlagE
Listing Certified Through2018-12-31

Packaging

NDC 15631-0261-0

100 PELLET in 1 VIAL, SINGLE-DOSE (15631-0261-0)
Marketing Start Date2018-01-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0261-0 [15631026100]

LACHESIS MUTUS PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-23

NDC 15631-0261-2 [15631026102]

LACHESIS MUTUS PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-23

NDC 15631-0261-1 [15631026101]

LACHESIS MUTUS PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-23

NDC 15631-0261-5 [15631026105]

LACHESIS MUTUS PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-23

NDC 15631-0261-4 [15631026104]

LACHESIS MUTUS PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-23

NDC 15631-0261-3 [15631026103]

LACHESIS MUTUS PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-23

Drug Details

Active Ingredients

IngredientStrength
LACHESIS MUTA VENOM8 [hp_X]/1

OpenFDA Data

SPL SET ID:f0fb484b-1495-47b6-893a-ed67b74fe55f
Manufacturer
UNII

NDC Crossover Matching brand name "LACHESIS MUTUS" or generic name "Lachesis Mutus"

NDCBrand NameGeneric Name
0220-3012Lachesis mutusLACHESIS MUTA VENOM
0220-3013Lachesis mutusLACHESIS MUTA VENOM
0220-3016Lachesis mutusLACHESIS MUTA VENOM
0220-3017Lachesis mutusLACHESIS MUTA VENOM
0220-3020Lachesis mutusLACHESIS MUTA VENOM
0220-3023Lachesis mutusLACHESIS MUTA VENOM
0220-3025Lachesis mutusLACHESIS MUTA VENOM
0220-3026Lachesis mutusLACHESIS MUTA VENOM
0220-3027Lachesis mutusLACHESIS MUTA VENOM
0220-3028Lachesis mutusLACHESIS MUTA VENOM
0220-3029Lachesis mutusLACHESIS MUTA VENOM
0220-3030Lachesis mutusLACHESIS MUTA VENOM
0360-0245LACHESIS MUTUSLACHESIS MUTA
10191-1457LACHESIS MUTUSBUSHMASTER VENOM
10191-1458LACHESIS MUTUSBUSHMASTER VENOM
10191-1459LACHESIS MUTUSBUSHMASTER VENOM
10191-1460LACHESIS MUTUSBUSHMASTER VENOM
10191-1461LACHESIS MUTUSBUSHMASTER SNAKE VENOM
15631-0261LACHESIS MUTUSLACHESIS MUTUS
15631-0620LACHESIS MUTUSLACHESIS MUTUS
53645-1530Lachesis MutusLachesis Mutus
55714-6306Lachesis mutusLachesis mutus
62106-6654LACHESIS MUTUSBushmaster
63083-7124Lachesis mutusLachesis mutus
68428-464Lachesis mutusLACHESIS MUTA VENOM
71919-399Lachesis mutusLACHESIS MUTA VENOM
76472-1150Lachesis MutusLACHESIS MUTA VENOM
76472-3022LACHESIS MUTUSLACHESIS MUTUS
44911-0388LachesisLachesis Mutus

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.