NDC 66576-336

Gilphex

Guaifenesin, Phenylephrine Hcl

Gilphex is a Oral Tablet in the Human Otc Drug category. It is labeled and distributed by Syntho Pharmaceuticals, Inc.. The primary component is Guaifenesin; Phenylephrine Hydrochloride.

Product ID66576-336_e1501276-6d45-6ae8-e053-2a95a90abfa7
NDC66576-336
Product TypeHuman Otc Drug
Proprietary NameGilphex
Generic NameGuaifenesin, Phenylephrine Hcl
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2022-05-05
Marketing CategoryOTC MONOGRAPH FINAL /
Application Numberpart341
Labeler NameSyntho Pharmaceuticals, Inc.
Substance NameGUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE
Active Ingredient Strength390 mg/1; mg/1
Pharm ClassesAdrenergic alpha1-Agonists [MoA], Decreased Respiratory Secretion Viscosity [PE], Expectorant [EPC], Increased Respiratory Secretions [PE], alpha-1 Adrenergic Agonist [EPC]
NDC Exclude FlagN
Listing Certified Through2023-12-31

Packaging

NDC 66576-336-01

100 TABLET in 1 BOTTLE (66576-336-01)
Marketing Start Date2022-05-05
NDC Exclude FlagN
Sample Package?N

Drug Details

NDC Crossover Matching brand name "Gilphex" or generic name "Guaifenesin, Phenylephrine Hcl"

NDCBrand NameGeneric Name
58552-336GilphexGuaifenesin, Phenylephrine HCl
66576-336GilphexGuaifenesin, Phenylephrine HCl
76864-209BACZOL EXPECTORANTGUAIFENESIN, PHENYLEPHRINE HCl
45737-606BiophexGuaifenesin, Phenylephrine HCl
58552-332Giltuss Sinus and Chest CongestionGuaifenesin, Phenylephrine HCl
0363-0542Mucus Relief PEGuaifenesin, Phenylephrine HCl
68016-686Mucus Relief PEGuaifenesin, Phenylephrine HCl
70000-0141Mucus Relief PE Sinus CongestionGuaifenesin, Phenylephrine HCl
59779-548Non-Drying Sinus PEGuaifenesin, Phenylephrine HCl
21130-927Sinus PEGuaifenesin, Phenylephrine HCl
50844-548Sinus Relief PEGuaifenesin, Phenylephrine HCl
54859-605Tusnel Pediatric DropsGuaifenesin, Phenylephrine HCl

Trademark Results [Gilphex]

Mark Image

Registration | Serial
Company
Trademark
Application Date
GILPHEX
GILPHEX
78096487 not registered Dead/Abandoned
Gil Pharmaceutical Corp.
2001-12-04

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