NDC 53002-0673

Doxycycline 100 mg capsule

On the label: RPK Pharmaceuticals, Inc.. It's repackaged: RPK Pharmaceuticals, Inc. rebottles it from Caraco Pharmaceutical Laboratories, Ltd.'s NDC 63304-616.

Where the pills inside were made

Repackaging site

• RPK Pharmaceuticals, Inc., Union City, California, United States · repackages it and relabels it

Recalls

• Apr 13, 2022 · Class II · Mckesson Medical-Surgical Inc. Corporate Office
  cGMP deviations: Temperature abuse
  Lots: McKesson Medical-Surgical (MMS) is not able to identify the particular lot number received by a particular consignee for the recalled prescription products. Each letter includes the date it was distributed to customers and the dates that impacted product may have been shipped to the customer.
• Mar 13, 2020 · Class II · Sun Pharmaceutical Industries, Inc.
  CGMP Deviations: Doxycycline capsules were not manufactured under Current Good Manufacturing Practice conditions.
  Lots: Lot #: AA39490, Exp 03/2021
• Mar 13, 2020 · Class II · Sun Pharmaceutical Industries, Inc.
  CGMP Deviations: Doxycycline capsules were not manufactured under Current Good Manufacturing Practice conditions.
  Lots: Lot #: 3983720, Exp 10/2020; 3990461, 3990464, 3990465, 3990466, 3990470, Exp 11/2020; AA42499, AA42510, AA44468, AA44470, Exp 04/2021; AA55073, AA55074, AA55075, Exp 05/2021; AA61486, Exp 06/2021

Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.

Product details

Generic drug

Doxycycline: every company that makes it

Form

capsule

Strength

100 mg

Approval

ANDA ANDA065053

On the market since

Dec 26, 2000

Package NDCs

53002-0673-0 53002-0673-1 53002-0673-2 53002-0673-3 53002-0673-4 53002-0673-5 53002-0673-6 53002-0673-7 53002-0673-9

Official label

DailyMed (National Library of Medicine), updated Mar 30, 2022

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