NDC 70005-006

Acetaminophen Tablets, 500 mg Extra Strength

Acetaminophen

Acetaminophen Tablets, 500 mg Extra Strength is a Oral Tablet in the Human Otc Drug category. It is labeled and distributed by We Care Distributors Inc.. The primary component is Acetaminophen.

• Product ID: 70005-006_af3f90ed-b08c-450e-80e0-2a477a5ca095
• NDC: 70005-006
• Product Type: Human Otc Drug
• Proprietary Name: Acetaminophen Tablets, 500 mg Extra Strength
• Generic Name: Acetaminophen
• Dosage Form: Tablet
• Route of Administration: ORAL
• Marketing Start Date: 2016-02-08
• Marketing Category: OTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL
• Application Number: part343
• Labeler Name: We Care Distributors Inc.
• Substance Name: ACETAMINOPHEN
• Active Ingredient Strength: 500 mg/1
• NDC Exclude Flag: N
• Listing Certified Through: 2019-12-31

Packaging

NDC 70005-006-02

2 POUCH in 1 POUCH (70005-006-02) > 2 TABLET in 1 POUCH

• Marketing Start Date: 2016-02-08
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 70005-006-02 [70005000602]

Acetaminophen Tablets, 500 mg Extra Strength TABLET

• Marketing Category: OTC monograph not final
• Application Number: part343
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2016-02-08
• Inactivation Date: 2020-01-31

NDC 70005-006-50 [70005000650]

Acetaminophen Tablets, 500 mg Extra Strength TABLET

• Marketing Category: OTC monograph not final
• Application Number: part343
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2016-02-08
• Inactivation Date: 2020-01-31

NDC 70005-006-25 [70005000625]

Acetaminophen Tablets, 500 mg Extra Strength TABLET

• Marketing Category: OTC monograph not final
• Application Number: part343
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2016-02-08
• Inactivation Date: 2020-01-31

Drug Details

Active Ingredients

Ingredient	Strength
ACETAMINOPHEN	500 mg/1

OpenFDA Data

• SPL SET ID: a180dcf9-1224-4425-872d-a341f72f9b72
• Manufacturer:
  • We Care Distributors Inc.
• UNII:
  • 362O9ITL9D
• RxNorm Concept Unique ID - RxCUI:
  • 198440

NDC Crossover Matching brand name "Acetaminophen Tablets, 500 mg Extra Strength" or generic name "Acetaminophen"

NDC	Brand Name	Generic Name
70005-006	Acetaminophen Tablets, 500 mg Extra Strength	Acetaminophen Tablets, 500 mg 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