M F1
Pill imprint M F1 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:
-
M F1
- Strength:
- 20 mg
- Color:
- Yellow
- Size:
- 8.00 mm
- Shape:
- Round
- Availability:
- Rx and/or OTC
- Inactive Ingredients:
- D&C Yellow No. 10 Aluminium Lake
FD&C Yellow No. 6 Aluminum Lake
hypromellose
lactose monohydrate
magnesium stearate
microcrystalline cellulose
polydextrose
polyethylene glycol
povidone
pregelatinized starch
sodium lauryl sulfate
sodium starch glycolate
titanium dioxide
triacetin
FD&C Blue No. 2 Aluminium Lake
- Drug Class:
- H2 antagonists
- Pregnancy Category:
- B - No proven risk in humans
- CSA Schedule:
- N - Not a controlled drug
- Manufacturer:
- Mylan Pharmaceuticals Inc.
- National Drug Code (NDC):
- 00378-3020
| NDC Code | Manufacturer / Repackager |
|---|---|
| 51079-0966 | UDL Laboratories Inc |
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
- Famotidine (AHFS DI)
- Equate Acid Controller Maximum Strength (FDA)
- Famotidine Drug Facts (FDA)
- Famotidine Injection (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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