Nifedipine 00904-7208

Product NDC

00904-7208

Manufacturer: Major Pharmaceuticals
Dosage Form: Tablet, Film Coated, Extended Release
Route: Oral
Product Type: Human Prescription Drug
Marketing Start: November 1, 2014
Listing Expires: December 31, 2027
Application: ANDA203126

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Active Ingredients

Ingredient	Strength
Nifedipine	30 mg/1

Drug Class

Dihydropyridine Calcium Channel Blocker [EPC]Calcium Channel Antagonists [MoA]Dihydropyridine Calcium Channel Blocker [EPC]

Packaging Options(2)

00904-7208-06

50 BLISTER PACK in 1 CARTON (0904-7208-06) / 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK

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00904-7208-61

100 BLISTER PACK in 1 CARTON (0904-7208-61) / 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK

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