7251 93
Pill imprint 7251 93 has been identified as Fexofenadine hydrochloride 30 mg.
Fexofenadine is used in the treatment of hay fever; urticaria and belongs to the drug class antihistamines. Risk cannot be ruled out during pregnancy.
Fexofenadine 30 mg is not subject to the Controlled Substances Act.
See also related documents.
Fexofenadine hydrochloride Images
- Imprint:
-
7251
93 - Strength:
- 30 mg
- Color:
- Orange
- Size:
- 9.00 mm
- Shape:
- Elliptical / Oval
- Availability:
- Prescription only
- Inactive Ingredients:
- silicon dioxide colloidal
croscarmellose sodium
hypromellose
ferrosoferric oxide
ferric oxide red
ferric oxide yellow
lactose monohydrate
magnesium stearate
microcrystalline cellulose
polyethylene glycol
povidone
titanium dioxide
- Drug Class:
- Antihistamines
- Pregnancy Category:
- C - Risk cannot be ruled out
- CSA Schedule:
- N - Not a controlled drug
- Manufacturer:
- Teva Pharmaceuticals USA
- National Drug Code (NDC):
- 00093-7251
| NDC Code | Manufacturer / Repackager |
|---|---|
| 23490-7428 | Palmetto State Pharmaceuticals Inc (repackager) |
Note: Inactive ingredients may vary.
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More Fexofenadine Hydrochloride resources
- Fexofenadine (Wolters Kluwer)
- Fexofenadine Orally Disintegrating Tablets (Wolters Kluwer)
- Fexofenadine Suspension (Wolters Kluwer)
- fexofenadine (Cerner Multum)
- fexofenadine (Micromedex) - Includes Dosage Information
- Fexofenadine Hydrochloride (AHFS DI)
- Fexofenadine (FDA)
- Fexofenadine Hydrochloride (Wolters Kluwer)
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