NDC 41163-520

Acetaminophen Gelcaps Extra Strength

Acetaminophen

Acetaminophen Gelcaps Extra Strength is a Oral Tablet, Coated in the Human Otc Drug category. It is labeled and distributed by Supervalu Inc.. The primary component is Acetaminophen.

• Product ID: 41163-520_133695bf-b41c-55ca-e054-00144ff8d46c
• NDC: 41163-520
• Product Type: Human Otc Drug
• Proprietary Name: Acetaminophen Gelcaps Extra Strength
• Generic Name: Acetaminophen
• Dosage Form: Tablet, Coated
• Route of Administration: ORAL
• Marketing Start Date: 2014-10-01
• Marketing Category: OTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL
• Application Number: part343
• Labeler Name: Supervalu Inc.
• Substance Name: ACETAMINOPHEN
• Active Ingredient Strength: 500 mg/1
• NDC Exclude Flag: E
• Listing Certified Through: 2018-12-31

Packaging

NDC 41163-520-01

1 BOTTLE, PLASTIC in 1 CARTON (41163-520-01) > 24 TABLET, COATED in 1 BOTTLE, PLASTIC

• Marketing Start Date: 2014-11-01
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 41163-520-03 [41163052003]

Acetaminophen Gelcaps Extra Strength TABLET, COATED

• Marketing Category: OTC monograph not final
• Application Number: part343
• Product Type: HUMAN OTC DRUG
• Billing Unit: EA
• Marketing Start Date: 2014-10-01

NDC 41163-520-07 [41163052007]

Acetaminophen Gelcaps Extra Strength TABLET, COATED

• Marketing Category: OTC monograph not final
• Application Number: part343
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2015-03-01
• Marketing End Date: 2016-10-31

NDC 41163-520-01 [41163052001]

Acetaminophen Gelcaps Extra Strength TABLET, COATED

• Marketing Category: OTC monograph not final
• Application Number: part343
• Product Type: HUMAN OTC DRUG
• Billing Unit: EA
• Marketing Start Date: 2014-11-01

NDC 41163-520-02 [41163052002]

Acetaminophen Gelcaps Extra Strength TABLET, COATED

• Marketing Category: OTC monograph not final
• Application Number: part343
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2015-03-01
• Marketing End Date: 2020-07-31

Drug Details

Active Ingredients

Ingredient	Strength
ACETAMINOPHEN	500 mg/1

OpenFDA Data

• SPL SET ID: 3588a3ef-a493-43ed-96e0-c259f0d087db
• Manufacturer:
  • Supervalu Inc.
• UNII:
  • 362O9ITL9D
• RxNorm Concept Unique ID - RxCUI:
  • 198440

NDC Crossover Matching brand name "Acetaminophen Gelcaps Extra Strength" or generic name "Acetaminophen"

NDC	Brand Name	Generic Name
41163-520	Acetaminophen Gelcaps Extra Strength	Acetaminophen Gelcaps Extra Strength
0121-0657	Acetaminophen	Acetaminophen
0113-7000	Basic Care acetaminophen	Acetaminophen
0113-7484	basic care acetaminophen	Acetaminophen
0113-7544	Basic Care Acetaminophen	Acetaminophen
0113-7130	basic care childrens pain and fever	Acetaminophen
0113-0020	good sense childrens pain and fever	Acetaminophen
0113-0212	Good Sense Childrens Pain and Fever	Acetaminophen
0113-0608	good sense childrens pain and fever	Acetaminophen
0113-0998	Good Sense Childrens Pain and Fever	Acetaminophen
0113-0161	Good Sense pain and fever	Acetaminophen
0113-0397	Good Sense Pain and Fever	acetaminophen
0113-0590	Good Sense Pain and Fever	acetaminophen
0113-0946	good sense pain and fever	Acetaminophen
0113-8959	Good Sense Pain and Fever	Acetaminophen
0113-0025	Good Sense Pain Relief	Acetaminophen
0113-0044	Good Sense Pain Relief	Acetaminophen
0113-0187	good sense pain relief	Acetaminophen
0113-0217	good sense pain relief	Acetaminophen
0113-0227	Good Sense Pain Relief	Acetaminophen
0113-0403	good sense pain relief	Acetaminophen
0113-0484	Good Sense Pain Relief	Acetaminophen
0113-0518	good sense pain relief	Acetaminophen
0113-0544	good sense pain relief	Acetaminophen
0113-1889	good sense pain relief	acetaminophen
0113-1975	Good Sense Pain Relief	Acetaminophen
0031-9301	Robitussin Direct Sore Throat Pain	acetaminophen