Pill imprint M 745 has been identified as Benazepril and hydrochlorothiazide 20 mg / 12.5 mg.

Benazepril/hydrochlorothiazide is used in the treatment of high blood pressure and belongs to the drug class antihypertensive combinations. There is positive evidence of human fetal risk during pregnancy.

Benazepril/hydrochlorothiazide 20 mg / 12.5 mg is not subject to the Controlled Substances Act.
See also related documents.

Inactive Ingredients:

• lactose anhydrous
• ferric oxide black
• silicon dioxide colloidal
• crospovidone
• hypromellose
• polydextrose
• polyethylene glycol
• pregelatinized starch
• stearic acid
• magnesium silicate
• titanium dioxide
• triacetin
• ferric oxide yellow

Drug Class:

Antihypertensive combinations

Pregnancy Category:

D – Positive evidence of risk

CSA Schedule:

N – Not a controlled drug

Manufacturer:

Mylan Pharmaceuticals Inc.

National Drug Code (NDC):

00378-4745

Drug: Mirtazapine
Strength(s): 30 mg
Imprint: 54 353
Color: Beige
Shape: Round

Pill imprint 54 353 has been identified as Mirtazapine 30 mg.

Mirtazapine is used in the treatment of depression; anxiety; insomnia; hot flashes; post traumatic stress disorder and belongs to the drug class tetracyclic antidepressants. Risk cannot be ruled out during pregnancy.

Mirtazapine 30 mg is not subject to the Controlled Substances Act.
See also related documents.

Drug: R-Tanna
Strength(s): chlorpheniramine tannate 9 mg / phenylephrine tannate 25 mg
Imprint: PRASCO 534
Color: Beige
Shape: Capsule-shape

Generic Name: chlorpheniramine/phenylephrine

Pill imprint PRASCO 534 has been identified as R-tanna chlorpheniramine tannate 9 mg / phenylephrine tannate 25 mg.

R-Tanna is used in the treatment of cold symptoms; hay fever and belongs to the drug class upper respiratory combinations. FDA has not classified the drug for risk during pregnancy.

R-Tanna chlorpheniramine tannate 9 mg / phenylephrine tannate 25 mg is not subject to the Controlled Substances Act.
See also related documents.

Pill imprint 93 896 has been identified as Famotidine 20 mg.

Famotidine is used in the treatment of stomach ulcer; peptic ulcer; gerd; 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.

Inactive Ingredients:

• silicon dioxide colloidal
• corn starch
• hydroxypropyl cellulose
• hypromellose
• ferric oxide red
• ferric oxide yellow
• lactose monohydrate
• magnesium stearate
• microcrystalline cellulose
• polyethylene glycol 4000
• pregelatinized corn starch
• titanium dioxide

Drug Class:

H2 antagonists

Pregnancy Category:

B – No proven risk in humans

CSA Schedule:

N – Not a controlled drug

Manufacturer:

Teva Pharmaceuticals USA

National Drug Code (NDC):

00093-0896

Drug: Famotidine
Strength(s): 20 mg
Imprint: W 936
Color: Beige
Shape: Barrel

Pill imprint W 936 has been identified as Famotidine 20 mg.

Famotidine is used in the treatment of stomach ulcer; peptic ulcer; gerd; 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.

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