NDC 0067-2000

Excedrin Extra Strength Pain Reliever

Acetaminophen, Aspirin (nsaid), And Caffeine

Excedrin Extra Strength Pain Reliever is a Oral Tablet, Film Coated in the Human Otc Drug category. It is labeled and distributed by Glaxosmithkline Consumer Healthcare Holdings (us) Llc. The primary component is Acetaminophen; Aspirin; Caffeine.

• Product ID: 0067-2000_66c08ddf-952d-4d4b-9b17-e8ea4269445e
• NDC: 0067-2000
• Product Type: Human Otc Drug
• Proprietary Name: Excedrin Extra Strength Pain Reliever
• Generic Name: Acetaminophen, Aspirin (nsaid), And Caffeine
• Dosage Form: Tablet, Film Coated
• Route of Administration: ORAL
• Marketing Start Date: 2006-09-27
• Marketing Category: OTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL
• Application Number: part343
• Labeler Name: GlaxoSmithKline Consumer Healthcare Holdings (US) LLC
• Substance Name: ACETAMINOPHEN; ASPIRIN; CAFFEINE
• Active Ingredient Strength: 250 mg/1; mg/1; mg/1
• NDC Exclude Flag: N
• Listing Certified Through: 2021-12-31

Packaging

NDC 0067-2000-02

2 TABLET, FILM COATED in 1 POUCH (0067-2000-02)

• Marketing Start Date: 2006-09-27
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 0067-2000-91 [00067200091]

Excedrin Extra Strength Pain Reliever TABLET, FILM COATED

• Marketing Category: OTC monograph not final
• Application Number: part343
• Product Type: HUMAN OTC DRUG
• Billing Unit: EA
• Marketing Start Date: 2006-09-27

NDC 0067-2000-83 [00067200083]

Excedrin Extra Strength Pain Reliever TABLET, FILM COATED

• Marketing Category: OTC monograph not final
• Application Number: part343
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2006-09-27

NDC 0067-2000-20 [00067200020]

Excedrin Extra Strength Pain Reliever TABLET, FILM COATED

• Marketing Category: OTC monograph not final
• Application Number: part343
• Product Type: HUMAN OTC DRUG
• Billing Unit: EA
• Marketing Start Date: 2006-09-27

NDC 0067-2000-77 [00067200077]

Excedrin Extra Strength Pain Reliever TABLET, FILM COATED

• Marketing Category: OTC monograph not final
• Application Number: part343
• Product Type: HUMAN OTC DRUG
• Billing Unit: EA
• Marketing Start Date: 2006-09-27

NDC 0067-2000-10 [00067200010]

Excedrin Extra Strength Pain Reliever TABLET, FILM COATED

• Marketing Category: OTC monograph not final
• Application Number: part343
• Product Type: HUMAN OTC DRUG
• Billing Unit: EA
• Marketing Start Date: 2006-09-27

NDC 0067-2000-50 [00067200050]

Excedrin Extra Strength Pain Reliever TABLET, FILM COATED

• Marketing Category: OTC monograph not final
• Application Number: part343
• Product Type: HUMAN OTC DRUG
• Billing Unit: EA
• Marketing Start Date: 2006-09-27

NDC 0067-2000-94 [00067200094]

Excedrin Extra Strength Pain Reliever TABLET, FILM COATED

• Marketing Category: OTC monograph not final
• Application Number: part343
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2006-09-27
• Marketing End Date: 2014-12-31

NDC 0067-2000-33 [00067200033]

Excedrin Extra Strength Pain Reliever TABLET, FILM COATED

• Marketing Category: OTC monograph not final
• Application Number: part343
• Product Type: HUMAN OTC DRUG
• Billing Unit: EA
• Marketing Start Date: 2006-09-27

NDC 0067-2000-24 [00067200024]

Excedrin Extra Strength Pain Reliever TABLET, FILM COATED

• Marketing Category: OTC monograph not final
• Application Number: part343
• Product Type: HUMAN OTC DRUG
• Billing Unit: EA
• Marketing Start Date: 2006-09-27

NDC 0067-2000-02 [00067200002]

Excedrin Extra Strength Pain Reliever TABLET, FILM COATED

• Marketing Category: OTC monograph not final
• Application Number: part343
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2006-09-27

NDC 0067-2000-07 [00067200007]

Excedrin Extra Strength Pain Reliever TABLET, FILM COATED

• Marketing Category: OTC monograph not final
• Application Number: part343
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2006-09-27
• Marketing End Date: 2014-12-31

NDC 0067-2000-30 [00067200030]

Excedrin Extra Strength Pain Reliever TABLET, FILM COATED

• Marketing Category: OTC monograph not final
• Application Number: part343
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2006-09-27

Drug Details

Active Ingredients

Ingredient	Strength
ACETAMINOPHEN	250 mg/1

OpenFDA Data

• SPL SET ID: a71074a6-cc19-4bb3-8c84-4e82a8906801
• Manufacturer:
  • GlaxoSmithKline Consumer Healthcare Holdings (US) LLC
• UNII:
  • 362O9ITL9D
  • R16CO5Y76E
  • 3G6A5W338E
• RxNorm Concept Unique ID - RxCUI:
  • 308297
  • 209468
• Pharm Class PE:
  • Decreased Prostaglandin Production [PE]
  • Decreased Platelet Aggregation [PE]
• PHarm Class EPC:
  • Nonsteroidal Anti-inflammatory Drug [EPC]
  • Platelet Aggregation Inhibitor [EPC]
• NUI Code:
  • N0000008832
  • N0000008836
  • N0000175721
  • N0000000160
  • N0000175578
  • N0000175722

NDC Crossover Matching brand name "Excedrin Extra Strength Pain Reliever" or generic name "Acetaminophen, Aspirin (nsaid), And Caffeine"

NDC	Brand Name	Generic Name
29485-8026	EXCEDRIN EXTRA STRENGTH PAIN RELIEVER	ACETAMINOPHEN, ASPIRIN, and CAFFEINE
29485-8027	EXCEDRIN EXTRA STRENGTH PAIN RELIEVER	ACETAMINOPHEN, ASPIRIN, and CAFFEINE
0067-2000	Excedrin	Acetaminophen, Aspirin (NSAID), and Caffeine
0067-2001	Excedrin	Acetaminophen, Aspirin (NSAID), and Caffeine
0067-8202	Excedrin	Acetaminophen, Aspirin (NSAID), and Caffeine
0067-8203	Excedrin	Acetaminophen, Aspirin (NSAID), and Caffeine
53808-0834	Excedrin	Acetaminophen, Aspirin (NSAID), and Caffeine
70518-3399	Excedrin	Acetaminophen, Aspirin (NSAID), and Caffeine
52904-868	Excedrin Extra Strength	acetaminophen, aspirin (nsaid), and caffeine
0067-8151	Excedrin Extra Strength and Excedrin Tension Headache	Acetaminophen, Aspirin (NSAID), and Caffeine