C 119
Pill imprint C 119 has been identified as Famotidine 20 mg.
Famotidine is used in the treatment of stomach ulcer; gerd; peptic ulcer; indigestion; erosive esophagitis (and more), and belongs to the drug class H2 antagonists. There is no proven risk in humans during pregnancy.
Famotidine 20 mg is not subject to the Controlled Substances Act.
See also related documents.
Famotidine Images
- Imprint:
-
C 119
- Strength:
- 20 mg
- Color:
- Yellow
- Size:
- 8.00 mm
- Shape:
- Round
- Availability:
- Rx and/or OTC
- Inactive Ingredients:
- silicon dioxide colloidal
magnesium stearate
microcrystalline cellulose
FD&C Yellow No. 6
corn starch
magnesium silicate
hypromellose
polyethylene glycol 400
ferric oxide yellow
titanium dioxide
- Drug Class:
- H2 antagonists
- Pregnancy Category:
- B - No proven risk in humans
- CSA Schedule:
- N - Not a controlled drug
- Manufacturer:
- Major Pharmaceuticals Inc.
- National Drug Code (NDC):
- 00904-5553
| NDC Code | Manufacturer / Repackager |
|---|---|
| 49884-0608 | Par Pharmaceutical |
| 55111-0119 | Dr. Reddy's Laboratories Inc. |
| 63739-0325 | McKesson Packaging Services |
| 66267-0543 | Nucare Pharmaceuticals Inc (repackager) |
| 68115-0138 | Dispensexpress Inc (repackager) |
| 66336-0355 | Dispensing Solutions Inc. (repackager) |
| 16590-0281 | Stat RX USA LLC (repackager) |
| 23490-5559 | Palmetto State Pharmaceuticals Inc (repackager) |
Note: Inactive ingredients may vary.
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More Famotidine resources
- Famotidine
- Famotidine (Wolters Kluwer)
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- Famotidine Solution (Wolters Kluwer)
- Famotidine Suspension (Wolters Kluwer)
- famotidine (Cerner Multum)
- famotidine (Micromedex) - Includes Dosage Information
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- Equate Acid Controller Maximum Strength (FDA)
- Famotidine Drug Facts (FDA)
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- Famotidine Tablets (FDA)
- Good Neighbor Acid Reducer (FDA)
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- Leader Acid Reducer Maximum Strength (FDA)
- Major Heartburn Relief Maximum Strength (FDA)
- Sunmark Acid Reducer (FDA)
- Topcare Acid Reducer (FDA)
- Famotidine (Wolters Kluwer)
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