OXAPROZIN (Page 7 of 7)

Oxaprozin product label

Do not use if seal is broken NDC 70332-310-01

14 tablets Oxaprozin 600 mg Tablets, USP Rx Only

(Each tablet contains 600 mg of Oxaprozin, USP)

Manufactured by:
Dr. Reddy’s Laboratories, Ltd
Bachepalli, 502 325 INDIA Store at 20°C (68° to 77°F)
Repackaged & Distributed By: Excursions permitted to 15° to 30°C (59° to 86°F)
California Pharmaceuticals, LLC
Camarillo, CA 93012

Usual Dosage: See accompanying information. pantoprazole sodium delayed-released tablets must not be split, chewed, or crushed before administration

CS157-A1 rev 0 LOT EXP

California Pharmaceuticals

CalifPharma Oxaprozin -- 14
(click image for full-size original)

NDC 70332-310-02 Do not use if seal is broken

60 tablets Oxaprozin 600 mg Tablets, USP Rx Only

(Each tablet contains 600 mg of Oxaprozin, USP)

Manufactured by:
Dr. Reddy’s Laboratories, Ltd
Bachepalli, 502 325 INDIA Store at 20°C (68° to 77°F)
Repackaged & Distributed By: Excursions permitted to 15° to 30°C (59° to 86°F)


California Pharmaceuticals, LLC
Camarillo, CA 93012

Usual Dosage: See accompanying information. pantoprazole sodium delayed-released tablets must not be split, chewed, or crushed before administration

CS 166-A1 rev 0 LOT EXP

California Pharmaceuticals

CalifPharma Oxaprozin -- 60
(click image for full-size original)
OXAPROZIN oxaprozin tablet, film coated
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:70332-310(NDC:55111-170)
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
OXAPROZIN (OXAPROZIN) OXAPROZIN 600 mg
Inactive Ingredients
Ingredient Name Strength
STARCH, CORN
D&C YELLOW NO. 10
FD&C YELLOW NO. 6
HYPROMELLOSES
LACTOSE MONOHYDRATE
MAGNESIUM STEARATE
CELLULOSE, MICROCRYSTALLINE
POLYDEXTROSE
POLYETHYLENE GLYCOLS
SODIUM STARCH GLYCOLATE TYPE A POTATO
TITANIUM DIOXIDE
TRIACETIN
Product Characteristics
Color yellow Score 2 pieces
Shape OVAL Size 19mm
Flavor Imprint Code C;01;70
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:70332-310-01 14 TABLET, FILM COATED in 1 BOTTLE None
2 NDC:70332-310-02 60 TABLET, FILM COATED in 1 BOTTLE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA075855 07/01/2017
Labeler — California Pharmaceuticals LLC (021420944)
Registrant — California Pharmaceuticals LLC (021420944)
Establishment
Name Address ID/FEI Operations
California Pharmaceuticals LLC 021420944 repack (70332-310)

Revised: 11/2017 California Pharmaceuticals LLC

All MedLibrary.org resources are included in as near-original form as possible, meaning that the information from the original provider has been rendered here with only typographical or stylistic modifications and not with any substantive alterations of content, meaning or intent.

This site is provided for educational and informational purposes only, in accordance with our Terms of Use, and is not intended as a substitute for the advice of a medical doctor, nurse, nurse practitioner or other qualified health professional.

Privacy Policy | Copyright © 2024. All Rights Reserved.