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Radha Pharmaceuticals, Inc. NDCs and Package Codes

This page lists NDC package records associated with labeler code 77771 (Radha 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

81
Package NDCs
51
Products
51
Active listings
0
Discontinued
15
Ingredients
2
Therapeutic classes
5
Dosage forms
0
With NADAC pricing

Portfolio

By therapeutic class
ANTIHYPERTENSIVES, VASODILATORS 4
PLATELET AGGREGATION INHIBITORS 1
Top ingredients
Celecoxib 8
bupropion hydrochloride 5
Buspirone hydrochloride 5
Hydralazine Hydrochloride 4
Carbidopa and Levodopa 4
Fluconazole 4
ATORVASTATIN CALCIUM 4
Fluoxetine Hydrochloride 3
Naproxen 3
Gabapentin 2
By dosage form
TABLET 20
CAPSULE 11
TABLET, FILM COATED 8
TABLET, FILM COATED, EXTENDED RELE... 8
TABLET, EXTENDED RELEASE 4

Browse records — 51 products

Drug / product Billing NDC NADAC / unit Status
ATORVASTATIN CALCIUM 80 mg/1 TABLET, FILM COATED Radha · NDC 77771-0454-05 · 500 TABLET, FILM COATED in 1 BOTTLE (77771-454-05) 77771-0454-05 — On market View →
ATORVASTATIN CALCIUM 20 mg/1 TABLET, FILM COATED Radha · NDC 77771-0452-05 · 500 TABLET, FILM COATED in 1 BOTTLE (77771-452-05) 77771-0452-05 — On market View →
ATORVASTATIN CALCIUM 10 mg/1 TABLET, FILM COATED Radha · NDC 77771-0451-10 · 1000 TABLET, FILM COATED in 1 BOTTLE (77771-451-10) 77771-0451-10 — On market View →
ATORVASTATIN CALCIUM 40 mg/1 TABLET, FILM COATED Radha · NDC 77771-0453-10 · 1000 TABLET, FILM COATED in 1 BOTTLE (77771-453-10) 77771-0453-10 — On market View →
Bupropion Hydrochloride (XL) 150 mg/1 TABLET, FILM COATED, EXTENDED RELEASE RADHA · NDC 77771-0144-05 · 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (77771-144-05) 77771-0144-05 — On market View →
Bupropion Hydrochloride (XL) 300 mg/1 TABLET, FILM COATED, EXTENDED RELEASE RADHA · NDC 77771-0145-05 · 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (77771-145-05) 77771-0145-05 — On market View →
Bupropion Hydrochloride SR 200 mg/1 TABLET, FILM COATED, EXTENDED RELEASE Radha · NDC 77771-0176-60 · 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (77771-176-60) 77771-0176-60 — On market View →
Bupropion Hydrochloride SR 100 mg/1 TABLET, FILM COATED, EXTENDED RELEASE Radha · NDC 77771-0174-05 · 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (77771-174-05) 77771-0174-05 — On market View →
Bupropion Hydrochloride SR 150 mg/1 TABLET, FILM COATED, EXTENDED RELEASE Radha · NDC 77771-0175-05 · 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (77771-175-05) 77771-0175-05 — On market View →
Buspirone hydrochloride 5 mg/1 TABLET Radha · NDC 77771-0234-01 · 100 TABLET in 1 BOTTLE (77771-234-01) 77771-0234-01 — On market View →
Buspirone hydrochloride 7.5 mg/1 TABLET Radha · NDC 77771-0235-01 · 100 TABLET in 1 BOTTLE (77771-235-01) 77771-0235-01 — On market View →
Buspirone hydrochloride 30 mg/1 TABLET Radha · NDC 77771-0238-60 · 60 TABLET in 1 BOTTLE (77771-238-60) 77771-0238-60 — On market View →
Buspirone hydrochloride 10 mg/1 TABLET Radha · NDC 77771-0236-01 · 100 TABLET in 1 BOTTLE (77771-236-01) 77771-0236-01 — On market View →
Buspirone hydrochloride 15 mg/1 TABLET Radha · NDC 77771-0237-05 · 500 TABLET in 1 BOTTLE (77771-237-05) 77771-0237-05 — On market View →
Carbidopa and Levodopa 25 mg/1; 100 mg/1 TABLET, EXTENDED RELEASE Radha · NDC 77771-0460-01 · 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (77771-460-01) 77771-0460-01 — On market View →
Carbidopa and Levodopa 50 mg/1; 200 mg/1 TABLET, EXTENDED RELEASE Radha · NDC 77771-0461-01 · 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (77771-461-01) 77771-0461-01 — On market View →
Carbidopa and Levodopa 50 mg/1; 200 mg/1 TABLET, EXTENDED RELEASE Radha · NDC 77771-0461-01 · 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (77771-461-01) 77771-0461-01 — On market View →
Carbidopa and Levodopa 25 mg/1; 100 mg/1 TABLET, EXTENDED RELEASE Radha · NDC 77771-0460-01 · 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (77771-460-01) 77771-0460-01 — On market View →
Celecoxib 100 mg/1 CAPSULE Radha · NDC 77771-0157-01 · 100 CAPSULE in 1 BOTTLE (77771-157-01) 77771-0157-01 — On market View →
Celecoxib 400 mg/1 CAPSULE Radha · NDC 77771-0159-60 · 60 CAPSULE in 1 BOTTLE (77771-159-60) 77771-0159-60 — On market View →
Celecoxib 200 mg/1 CAPSULE Radha · NDC 77771-0158-01 · 100 CAPSULE in 1 BOTTLE (77771-158-01) 77771-0158-01 — On market View →
Celecoxib 50 mg/1 CAPSULE Radha · NDC 77771-0156-60 · 60 CAPSULE in 1 BOTTLE (77771-156-60) 77771-0156-60 — On market View →
Celecoxib 400 mg/1 CAPSULE Radha · NDC 77771-0159-60 · 60 CAPSULE in 1 BOTTLE (77771-159-60) 77771-0159-60 — On market View →
Celecoxib 200 mg/1 CAPSULE Radha · NDC 77771-0158-01 · 100 CAPSULE in 1 BOTTLE (77771-158-01) 77771-0158-01 — On market View →
Celecoxib 100 mg/1 CAPSULE Radha · NDC 77771-0157-01 · 100 CAPSULE in 1 BOTTLE (77771-157-01) 77771-0157-01 — On market View →
Celecoxib 50 mg/1 CAPSULE Radha · NDC 77771-0156-60 · 60 CAPSULE in 1 BOTTLE (77771-156-60) 77771-0156-60 — On market View →
Clopidogrel bisulfate 300 mg/1 TABLET, FILM COATED RADHA · NDC 77771-0121-05 · 500 TABLET, FILM COATED in 1 BOTTLE (77771-121-05) 77771-0121-05 — On market View →
Clopidogrel bisulfate 75 mg/1 TABLET, FILM COATED RADHA · NDC 77771-0124-10 · 1000 TABLET, FILM COATED in 1 BOTTLE (77771-124-10) 77771-0124-10 — On market View →
fexofenadine hcl 60 mg/1 TABLET, FILM COATED Radha · NDC 77771-0201-01 · 100 TABLET, FILM COATED in 1 BOTTLE (77771-201-01) 77771-0201-01 — On market View →
fexofenadine hcl 180 mg/1 TABLET, FILM COATED Radha · NDC 77771-0202-01 · 100 TABLET, FILM COATED in 1 BOTTLE (77771-202-01) 77771-0202-01 — 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.