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Preferred Pharmaceuticals Inc. NDCs and Package Codes

This page lists NDC package records associated with labeler code 68788 (Preferred Pharmaceuticals Inc.) — including active listings, ingredients, drug names, strengths, dosage forms, package sizes, pricing data when available, and links to each individual NDC page.

Key stats

3,340
Package NDCs
1,237
Products
1,233
Active listings
4
Discontinued
322
Ingredients
0
Therapeutic classes
39
Dosage forms
0
With NADAC pricing

Portfolio

Top ingredients
LEVOTHYROXINE SODIUM 28
Ibuprofen 19
METFORMIN HYDROCHLORIDE 18
Amoxicillin 16
gabapentin 16
diclofenac sodium 14
PredniSONE 14
Amoxicillin and Clavulanate Potass... 13
Acetaminophen 13
Pravastatin sodium 13
By dosage form
TABLET 419
TABLET, FILM COATED 250
CAPSULE 126
CREAM 72
SOLUTION 49
TABLET, EXTENDED RELEASE 31
SUSPENSION 27
TABLET, COATED 26

Browse records — 1,237 products

Drug / product Billing NDC NADAC / unit Status
Omeprazole 20 mg/1 CAPSULE, DELAYED RELEASE Preferred · NDC 68788-8805-01 · 100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-8805-1) 68788-8805-01 — On market View →
Omeprazole 20 mg/1 CAPSULE, DELAYED RELEASE Preferred · NDC 68788-8864-01 · 100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-8864-1) 68788-8864-01 — On market View →
Omeprazole 20 mg/1 CAPSULE, DELAYED RELEASE Preferred · NDC 68788-6881-01 · 100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-6881-1) 68788-6881-01 — On market View →
Omeprazole 20 mg/1 CAPSULE, DELAYED RELEASE Preferred · NDC 68788-4104-01 · 100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-4104-1) 68788-4104-01 — On market View →
Omeprazole 20 mg/1 CAPSULE, DELAYED RELEASE Preferred · NDC 68788-6881-01 · 100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-6881-1) 68788-6881-01 — On market View →
Ondansetron 4 mg/1 TABLET, ORALLY DISINTEGRATING Preferred · NDC 68788-8666-01 · Q0162 · 30 TABLET, ORALLY DISINTEGRATING in 1 PACKET (68788-8666-1) 68788-8666-01 — On market View →
Ondansetron 8 mg/1 TABLET, ORALLY DISINTEGRATING Preferred · NDC 68788-7565-01 · Q0162 · 10 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (68788-7565-1) 68788-7565-01 — On market View →
Ondansetron 4 mg/1 TABLET, ORALLY DISINTEGRATING Preferred · NDC 68788-7644-01 · Q0162 · 10 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (68788-7644-1) 68788-7644-01 — On market View →
Ondansetron 8 mg/1 TABLET, ORALLY DISINTEGRATING Preferred · NDC 68788-4133-01 · 10 TABLET, ORALLY DISINTEGRATING in 1 BOX, UNIT-DOSE (68788-4133-1) 68788-4133-01 — On market View →
Ondansetron 8 mg/1 TABLET, ORALLY DISINTEGRATING Preferred · NDC 68788-9559-01 · 10 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (68788-9559-1) 68788-9559-01 — On market View →
Ondansetron 4 mg/1 TABLET, ORALLY DISINTEGRATING Preferred · NDC 68788-8666-01 · Q0162 · 30 TABLET, ORALLY DISINTEGRATING in 1 PACKET (68788-8666-1) 68788-8666-01 — On market View →
Ondansetron 4 mg/1 TABLET, ORALLY DISINTEGRATING Preferred · NDC 68788-7644-01 · Q0162 · 10 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (68788-7644-1) 68788-7644-01 — On market View →
Ondansetron 8 mg/1 TABLET, ORALLY DISINTEGRATING Preferred · NDC 68788-7565-01 · Q0162 · 10 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (68788-7565-1) 68788-7565-01 — On market View →
Ondansetron Hydrochloride 4 mg/1 TABLET, FILM COATED Preferred · NDC 68788-9368-01 · Q0162 · 10 TABLET, FILM COATED in 1 BOTTLE (68788-9368-1) 68788-9368-01 — On market View →
Ondansetron Hydrochloride 8 mg/1 TABLET, FILM COATED Preferred · NDC 68788-9402-01 · Q0162 · 10 TABLET, FILM COATED in 1 BOTTLE (68788-9402-1) 68788-9402-01 — On market View →
Ondansetron Hydrochloride 4 mg/1 TABLET, FILM COATED Preferred · NDC 68788-8651-01 · Q0162 · 10 TABLET, FILM COATED in 1 BOTTLE (68788-8651-1) 68788-8651-01 — On market View →
Ondansetron Hydrochloride 8 mg/1 TABLET, FILM COATED Preferred · NDC 68788-8582-01 · Q0162 · 10 TABLET, FILM COATED in 1 BOTTLE (68788-8582-1) 68788-8582-01 — On market View →
Ondansetron Hydrochloride 8 mg/1 TABLET, FILM COATED Preferred · NDC 68788-8582-01 · Q0162 · 10 TABLET, FILM COATED in 1 BOTTLE (68788-8582-1) 68788-8582-01 — On market View →
Ondansetron Hydrochloride 8 mg/1 TABLET, FILM COATED Preferred · NDC 68788-9402-01 · Q0162 · 10 TABLET, FILM COATED in 1 BOTTLE (68788-9402-1) 68788-9402-01 — On market View →
Ondansetron Hydrochloride 4 mg/1 TABLET, FILM COATED Preferred · NDC 68788-9368-01 · Q0162 · 10 TABLET, FILM COATED in 1 BOTTLE (68788-9368-1) 68788-9368-01 — On market View →
Orphenadrine Citrate 100 mg/1 TABLET, EXTENDED RELEASE Preferred · NDC 68788-9138-01 · 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-9138-1) 68788-9138-01 — On market View →
Orphenadrine Citrate 100 mg/1 TABLET, EXTENDED RELEASE Preferred · NDC 68788-9138-01 · 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-9138-1) 68788-9138-01 — On market View →
Oseltamivir Phosphate 75 mg/1 CAPSULE Preferred · NDC 68788-8122-01 · 10 CAPSULE in 1 BLISTER PACK (68788-8122-1) 68788-8122-01 — On market View →
Oseltamivir Phosphate 6 mg/mL FOR SUSPENSION Preferred · NDC 68788-7600-06 · 1 BOTTLE in 1 CARTON (68788-7600-6) / 60 mL in 1 BOTTLE 68788-7600-06 — On market View →
Oseltamivir phosphate 6 mg/mL FOR SUSPENSION Preferred · NDC 68788-8123-06 · 1 POUCH in 1 CARTON (68788-8123-6) / 1 BOTTLE in 1 POUCH / 60 mL in 1 BOTTLE 68788-8123-06 — On market View →
OSELTAMIVIR PHOSPHATE 75 mg/1 CAPSULE Preferred · NDC 68788-4066-01 · 1 BLISTER PACK in 1 CARTON (68788-4066-1) / 10 CAPSULE in 1 BLISTER PACK 68788-4066-01 — On market View →
Oseltamivir phosphate 75 mg/1 CAPSULE Preferred · NDC 68788-8309-01 · 1 BLISTER PACK in 1 CARTON (68788-8309-1) / 10 CAPSULE in 1 BLISTER PACK 68788-8309-01 — On market View →
Oseltamivir phosphate 75 mg/1 CAPSULE Preferred · NDC 68788-8831-01 · 1 BLISTER PACK in 1 CARTON (68788-8831-1) / 10 CAPSULE in 1 BLISTER PACK 68788-8831-01 — On market View →
Oseltamivir phosphate 75 mg/1 CAPSULE Preferred · NDC 68788-8309-01 · 1 BLISTER PACK in 1 CARTON (68788-8309-1) / 10 CAPSULE in 1 BLISTER PACK 68788-8309-01 — On market View →
Oseltamivir Phosphate 75 mg/1 CAPSULE Preferred · NDC 68788-8122-01 · 10 CAPSULE in 1 BLISTER PACK (68788-8122-1) 68788-8122-01 — On market View →
Where does this data come from?
NDC package records, ingredients, strengths and forms come from the openFDA NDC Directory, grouped by the 5-digit labeler code; pricing is CMS NADAC. This is a factual data directory, not a manufacturer marketing page.