NDC 37662-2318

Sulphur

Sulphur

Sulphur is a Oral Pellet in the Human Otc Drug category. It is labeled and distributed by Hahnemann Laboratories, Inc.. The primary component is Sulfur.

Product ID37662-2318_f208f88c-3c4e-f177-e053-2995a90aba01
NDC37662-2318
Product TypeHuman Otc Drug
Proprietary NameSulphur
Generic NameSulphur
Dosage FormPellet
Route of AdministrationORAL
Marketing Start Date2023-01-11
Marketing CategoryUNAPPROVED HOMEOPATHIC /
Labeler NameHahnemann Laboratories, INC.
Substance NameSULFUR
Active Ingredient Strength500 [hp_C]/1
NDC Exclude FlagN
Listing Certified Through2024-12-31

Packaging

NDC 37662-2318-1

200 PELLET in 1 VIAL, GLASS (37662-2318-1)
Marketing Start Date2023-01-11
NDC Exclude FlagN
Sample Package?N

Drug Details

NDC Crossover Matching brand name "Sulphur" or generic name "Sulphur"

NDCBrand NameGeneric Name
0220-4813SulphurSULFUR
0220-4816SulphurSULFUR
0220-4817SulphurSULFUR
0220-4820SulphurSULFUR
0220-4821SulphurSULFUR
0220-4823SulphurSULFUR
0220-4826SulphurSULFUR
0220-4827SulphurSULFUR
0220-4828SulphurSULFUR
0220-4829SulphurSULFUR
0220-4830SulphurSULFUR
0220-4831SulphurSULFUR
0360-0368SULPHURSULPHOR
0360-0369SULPHURSULPHUR
10191-1578SULPHURSULFUR
10191-1585SULPHURSULFUR
10191-1587SULPHURSULFUR
10191-1589SULPHURSULFUR
15631-0420SULPHURSULPHUR
15631-0692SULPHURSULPHUR
15631-2322SULPHURSULPHUR
37662-2313SulphurSulphur
37662-2314SulphurSulphur
37662-2315SulphurSulphur
37662-2316SulphurSulphur
37662-2317SulphurSulphur
37662-2318SulphurSulphur
37662-2319SulphurSulphur
37662-2320SulphurSulphur
37662-2321SulphurSulphur
44911-0394SulphurSulphur
54973-0627SULPHURSULFUR
54973-2927SULPHURSULFUR
55714-6516SulphurSulphur
68428-655SulphurSulphur
60512-1047SULPHURSULPHUR
62106-5316SULPHURSULPHUR
76472-1165SULPHURSULPHUR
55714-7516SulphurSulphur
0295-7300ProsaceaSulphur
52389-173ProsaceaSulphur
43406-0472Sulphur 30CSulphur
51439-004Treatment 101Sulphur

Trademark Results [Sulphur]

Mark Image

Registration | Serial
Company
Trademark
Application Date
SULPHUR
SULPHUR
79280963 not registered Live/Pending
H Sulphur Corp.
2020-01-07

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