51660-037 : Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride Oral Tablet, Film Coated, Extended Release

NDC:	51660-037
Labeler:	Ohm Laboratories Inc.
Product Type:	Human OTC Drug
Drug Name:	Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride
Dosage Form:	Oral Tablet, Film Coated, Extended Release
Application #:	ANDA090818
Rev. Date:	Mar 1, 2018

Appearance:

Markings:	724
Shapes:	Capsule
Colors:	White / Yellow
Size (mm):	17
Segments: ^*	1
^* Segments = the number of equally sized pieces which the pill can be broken into. In this case, a value of 1 indicates a solid pill with no score lines.

NDC Package Codes:

51660-037-21: 1 BLISTER PACK IN 1 CARTON (51660‑037‑21) > 20 TABLET, FILM COATED, EXTENDED RELEASE IN 1 BLISTER PACK
51660-037-31: 1 BLISTER PACK IN 1 CARTON (51660‑037‑31) > 30 TABLET, FILM COATED, EXTENDED RELEASE IN 1 BLISTER PACK

Active Ingredients:

Fexofenadine Hydrochloride
Pseudoephedrine Hydrochloride

Dosage Strength:

60 mg
120 mg

Inactive Ingredients:

Lactose Monohydrate
Microcrystalline Cellulose
Croscarmellose Sodium
Povidone K30
Magnesium Stearate
Dibasic Calcium Phosphate Dihydrate
Silicon Dioxide
Ethylcellulose, Unspecified
Ferric Oxide Yellow
Stearic Acid
Hypromellose, Unspecified
Polyethylene Glycol, Unspecified /

Pharmaceutical Classes:

Adrenergic alpha-Agonists [MoA]
Histamine H1 Receptor Antagonists [MoA]
Histamine-1 Receptor Antagonist [EPC]
alpha-Adrenergic Agonist [EPC]

NDC QR Code

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Note: The RxChat NDC Database uses publicly available data from the FDA and the U.S. National Library of Medicine (NLM); The NLM is not responsible for the data presented and does not endorse or recommend this or any other product. While we make every effort to ensure that the information presented is accurate, you should assume that all results are unvalidated. To report any errors or inconsistencies please contact us.