NDC 15127-972

Pain Reliever Extra Strength Non Aspirin

Acetaminophen

Pain Reliever Extra Strength Non Aspirin is a Oral Tablet, Film Coated in the Human Otc Drug category. It is labeled and distributed by L&r Distributors, Inc.. The primary component is Acetaminophen.

• Product ID: 15127-972_83fe0b74-7fd0-4844-b0dd-a5f61ff55b53
• NDC: 15127-972
• Product Type: Human Otc Drug
• Proprietary Name: Pain Reliever Extra Strength Non Aspirin
• Generic Name: Acetaminophen
• Dosage Form: Tablet, Film Coated
• Route of Administration: ORAL
• Marketing Start Date: 2005-12-11
• Marketing Category: OTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL
• Application Number: part343
• Labeler Name: L&R Distributors, Inc.
• Substance Name: ACETAMINOPHEN
• Active Ingredient Strength: 500 mg/1
• NDC Exclude Flag: N
• Listing Certified Through: 2019-12-31

Packaging

NDC 15127-972-01

1 BOTTLE in 1 CARTON (15127-972-01) > 100 TABLET, FILM COATED in 1 BOTTLE

• Marketing Start Date: 2005-12-11
• Marketing End Date: 2021-08-03
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 15127-972-24 [15127097224]

Pain Reliever Extra Strength Non Aspirin TABLET, FILM COATED

• Marketing Category: OTC MONOGRAPH NOT FINAL
• Application Number: part343
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2005-12-11
• Marketing End Date: 2021-08-03

NDC 15127-972-50 [15127097250]

Pain Reliever Extra Strength Non Aspirin TABLET, FILM COATED

• Marketing Category: OTC MONOGRAPH NOT FINAL
• Application Number: part343
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2005-12-11
• Marketing End Date: 2021-08-03

NDC 15127-972-01 [15127097201]

Pain Reliever Extra Strength Non Aspirin TABLET, FILM COATED

• Marketing Category: OTC MONOGRAPH NOT FINAL
• Application Number: part343
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2005-12-11
• Marketing End Date: 2021-08-03

NDC 15127-972-08 [15127097208]

Pain Reliever Extra Strength Non Aspirin TABLET, FILM COATED

• Marketing Category: OTC MONOGRAPH NOT FINAL
• Application Number: part343
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2005-12-11
• Marketing End Date: 2014-07-08

Drug Details

Active Ingredients

Ingredient	Strength
ACETAMINOPHEN	500 mg/1

OpenFDA Data

• SPL SET ID: 6de2e5cd-dd30-4cba-984d-3ef8332a5609
• Manufacturer:
  • L&R Distributors, Inc.
• UNII:
  • 362O9ITL9D
• RxNorm Concept Unique ID - RxCUI:
  • 198440
• UPC Code:
  • 0015127018333

NDC Crossover Matching brand name "Pain Reliever Extra Strength Non Aspirin" or generic name "Acetaminophen"

NDC	Brand Name	Generic Name
15127-972	Pain Reliever Extra Strength Non Aspirin	Pain Reliever Extra Strength Non Aspirin
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