NDC 0280-4000

Alka-Seltzer Original

Anhydrous Citric Acid, Aspirin, And Sodium Bicarbonate

Alka-Seltzer Original is a Oral Tablet, Effervescent in the Human Otc Drug category. It is labeled and distributed by Bayer Healthcare Llc.. The primary component is Anhydrous Citric Acid; Aspirin; Sodium Bicarbonate.

• Product ID: 0280-4000_4f5a429f-013e-0e39-e054-00144ff88e88
• NDC: 0280-4000
• Product Type: Human Otc Drug
• Proprietary Name: Alka-Seltzer Original
• Generic Name: Anhydrous Citric Acid, Aspirin, And Sodium Bicarbonate
• Dosage Form: Tablet, Effervescent
• Route of Administration: ORAL
• Marketing Start Date: 2010-03-02
• Marketing Category: OTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL
• Application Number: part343
• Labeler Name: Bayer HealthCare LLC.
• Substance Name: ANHYDROUS CITRIC ACID; ASPIRIN; SODIUM BICARBONATE
• Active Ingredient Strength: 1000 mg/1; mg/1; mg/1
• NDC Exclude Flag: N
• Listing Certified Through: 2019-12-31

Packaging

NDC 0280-4000-01

6 POUCH in 1 CARTON (0280-4000-01) > 2 TABLET, EFFERVESCENT in 1 POUCH

• Marketing Start Date: 2012-10-10
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 0280-4000-03 [00280400003]

Alka-Seltzer Original TABLET, EFFERVESCENT

• Marketing Category: OTC monograph not final
• Application Number: part343
• Product Type: HUMAN OTC DRUG
• Billing Unit: EA
• Marketing Start Date: 2012-10-10

NDC 0280-4000-04 [00280400004]

Alka-Seltzer Original TABLET, EFFERVESCENT

• Marketing Category: OTC monograph not final
• Application Number: part343
• Product Type: HUMAN OTC DRUG
• Billing Unit: EA
• Marketing Start Date: 2012-10-10

NDC 0280-4000-02 [00280400002]

Alka-Seltzer Original TABLET, EFFERVESCENT

• Marketing Category: OTC monograph not final
• Application Number: part343
• Product Type: HUMAN OTC DRUG
• Billing Unit: EA
• Marketing Start Date: 2012-10-10

NDC 0280-4000-07 [00280400007]

Alka-Seltzer Original TABLET, EFFERVESCENT

• Marketing Category: OTC monograph not final
• Application Number: part343
• Product Type: HUMAN OTC DRUG
• Billing Unit: EA
• Marketing Start Date: 2012-10-10

NDC 0280-4000-01 [00280400001]

Alka-Seltzer Original TABLET, EFFERVESCENT

• Marketing Category: OTC monograph not final
• Application Number: part343
• Product Type: HUMAN OTC DRUG
• Billing Unit: EA
• Marketing Start Date: 2012-10-10

Drug Details

Active Ingredients

Ingredient	Strength
ANHYDROUS CITRIC ACID	1000 mg/1

OpenFDA Data

• SPL SET ID: 5be36a7f-7d1f-468d-9c29-92c8cd3ef1bc
• Manufacturer:
  • Bayer HealthCare LLC.
• UNII:
  • XF417D3PSL
  • 8MDF5V39QO
  • R16CO5Y76E
• RxNorm Concept Unique ID - RxCUI:
  • 1536680
  • 1536675
• 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 "Alka-Seltzer Original" or generic name "Anhydrous Citric Acid, Aspirin, And Sodium Bicarbonate"

NDC	Brand Name	Generic Name
0280-4000	Alka-Seltzer Original	ANHYDROUS CITRIC ACID, ASPIRIN, and SODIUM BICARBONATE
29485-7535	ALKA-SELTZER ORIGINAL	anhydrous citric acid, aspirin, and sodium bicarbonate tablet, effervescent
65662-005	Alka-Seltzer Original	anhydrous citric acid, aspirin, and sodium bicarbonate
70262-304	Alka-Seltzer Original	ANHYDROUS CITRIC ACID, ASPIRIN, and SODIUM BICARBONATE
70264-014	Alka-Seltzer Original	ANHYDROUS CITRIC ACID, ASPIRIN, and SODIUM BICARBONATE
50269-307	Alka Seltzer Originial 1s Blister Pack	ANHYDROUS CITRIC ACID, ASPIRIN, and SODIUM BICARBONATE
66715-9703	Alka-Seltzer	Anhydrous Citric Acid, Aspirin, and Sodium Bicarbonate
0280-0084	Alka-Seltzer Hangover Relief	ANHYDROUS CITRIC ACID, ASPIRIN, and SODIUM BICARBONATE