Logo Zenith 50 mg 2130
Pill imprint Logo Zenith 50 mg 2130 has been identified as Nitrofurantoin macrocrystals 50 mg.
Nitrofurantoin is used in the treatment of urinary tract infection; bladder infection; prevention of bladder infection and belongs to the drug class urinary anti-infectives. There is no proven risk in humans during pregnancy.
Nitrofurantoin 50 mg is not subject to the Controlled Substances Act.
See also related documents.
Nitrofurantoin macrocrystals Images
- Imprint:
-
Logo Zenith 50 mg
2130 - Strength:
- 50 mg
- Color:
- Pink & White
- Size:
- 16.00 mm
- Shape:
- Capsule-shape
- Availability:
- Prescription only
- Inactive Ingredients:
- corn starch
ferrosoferric oxide
D&C Yellow No. 10
FD&C Blue No. 1
FD&C Blue No. 2
FD&C Red No. 40
aluminum oxide
D&C Red No. 33
gelatin
lactose monohydrate
silicon dioxide
sodium lauryl sulfate
magnesium silicate
titanium dioxide
- Drug Class:
- Urinary anti-infectives
- Pregnancy Category:
- B - No proven risk in humans
- CSA Schedule:
- N - Not a controlled drug
- Manufacturer:
- Teva Pharmaceuticals USA
- National Drug Code (NDC):
- 00093-2130
| NDC Code | Manufacturer / Repackager |
|---|---|
| 54569-0181 | A S Medication Solutions LLC (repackager) |
| 55289-0186 | PDRX Pharmaceuticals Inc (repackager) |
| 54868-0107 | Physicians Total Care Inc (repackager) |
Note: Inactive ingredients may vary.
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More Nitrofurantoin Macrocrystals resources
- Nitrofurantoin
- Nitrofurantoin (Wolters Kluwer)
- Nitrofurantoin Suspension (Wolters Kluwer)
- nitrofurantoin (Cerner Multum)
- Novo-Furan Suspension (Micromedex) - Includes Dosage Information
- nitrofurantoin (Micromedex) - Includes Dosage Information
- Nitrofurantoin (AHFS DI)
- Nitrofurantoin Capsules (FDA)
- Nitrofurantoin Macrocrystals (FDA)
- Nitrofurantoin Oral Suspension (FDA)
- Nitrofurantoin (Wolters Kluwer)
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