018
Pill imprint 018 has been identified as Fexofenadine hydrochloride 180 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 180 mg is not subject to the Controlled Substances Act.
See also related documents.
Fexofenadine hydrochloride Images
- Imprint:
-
018
- Strength:
- 180 mg
- Color:
- Orange
- Size:
- 17.00 mm
- Shape:
- Elliptical / Oval
- Availability:
- Prescription only
- Inactive Ingredients:
- croscarmellose sodium
magnesium stearate
microcrystalline cellulose
pregelatinized starch
hypromellose
polyethylene glycol
povidone
silicon dioxide
titanium dioxide
- Drug Class:
- Antihistamines
- Pregnancy Category:
- C - Risk cannot be ruled out
- CSA Schedule:
- N - Not a controlled drug
- Manufacturer:
- Prasco Laboratories
- National Drug Code (NDC):
- 66993-0109
| NDC Code | Manufacturer / Repackager |
|---|---|
| 49999-0772 | Lake Erie Medical and Surgical Supply (repackager) |
| 54569-5738 | A S Medication Solutions LLC (repackager) |
| 54868-5409 | Physicians Total Care Inc (repackager) |
| 16590-0536 | Stat RX USA LLC (repackager) |
| 53002-1409 | Pharmedix (repackager) |
Note: Inactive ingredients may vary.
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)


