NDC 75920-0464

Blowfish

Aspirin, Caffeine

Blowfish is a Oral Tablet, Effervescent in the Human Otc Drug category. It is labeled and distributed by Rally Labs Llc. The primary component is Aspirin; Caffeine.

• Product ID: 75920-0464_527dd364-1f24-48c2-e054-00144ff8d46c
• NDC: 75920-0464
• Product Type: Human Otc Drug
• Proprietary Name: Blowfish
• Generic Name: Aspirin, Caffeine
• Dosage Form: Tablet, Effervescent
• Route of Administration: ORAL
• Marketing Start Date: 2011-07-23
• Marketing Category: OTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL
• Application Number: part343
• Labeler Name: Rally Labs LLC
• Substance Name: ASPIRIN; CAFFEINE
• Active Ingredient Strength: 500 mg/1; mg/1
• NDC Exclude Flag: N
• Listing Certified Through: 2019-12-31

Packaging

NDC 75920-0464-1

2 TABLET, EFFERVESCENT in 1 BOX (75920-0464-1)

• Marketing Start Date: 2011-07-23
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 75920-0464-4 [75920046404]

Blowfish TABLET, EFFERVESCENT

• Marketing Category: OTC monograph not final
• Application Number: part343
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2017-11-30

NDC 75920-0464-2 [75920046402]

Blowfish TABLET, EFFERVESCENT

• Marketing Category: OTC monograph not final
• Application Number: part343
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2017-11-30

NDC 75920-0464-1 [75920046401]

Blowfish TABLET, EFFERVESCENT

• Marketing Category: OTC monograph not final
• Application Number: part343
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2011-07-23

NDC 75920-0464-6 [75920046406]

Blowfish TABLET, EFFERVESCENT

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

NDC 75920-0464-8 [75920046408]

Blowfish TABLET, EFFERVESCENT

• Marketing Category: OTC monograph not final
• Application Number: part343
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2011-07-23

Drug Details

Active Ingredients

Ingredient	Strength
ASPIRIN	500 mg/1

OpenFDA Data

• SPL SET ID: 0d3798bc-04ef-584e-821b-7aa76036b7d1
• Manufacturer:
  • Rally Labs LLC
• UNII:
  • R16CO5Y76E
  • 3G6A5W338E
• RxNorm Concept Unique ID - RxCUI:
  • 1537019
• Pharm Class PE:
  • Decreased Prostaglandin Production [PE]
  • Decreased Platelet Aggregation [PE]
• PHarm Class EPC:
  • Nonsteroidal Anti-inflammatory Drug [EPC]
  • Platelet Aggregation Inhibitor [EPC]
• UPC Code:
  • 0375920000011
• NUI Code:
  • N0000008832
  • N0000008836
  • N0000175721
  • N0000000160
  • N0000175578
  • N0000175722

NDC Crossover Matching brand name "Blowfish" or generic name "Aspirin, Caffeine"

NDC	Brand Name	Generic Name
75920-0464	Blowfish	Aspirin, Caffeine
33992-0413	Back and Body	Aspirin, Caffeine
41250-143	Back and Body	Aspirin, Caffeine
50844-413	Back and Body	Aspirin, Caffeine
55910-134	Back and Body	Aspirin, Caffeine
59779-143	Back and Body	Aspirin, Caffeine
70000-0127	Back and Body	Aspirin, Caffeine
0363-0431	Extra Strength Back and Body	Aspirin, Caffeine
11822-4130	pain relief back and body	Aspirin, Caffeine
73156-010	RU-21 HANGOVER RELIEF	ASPIRIN, CAFFEINE
73408-821	Thompson XS Pain Ache	Aspirin, Caffeine
49314-8218	Unishield Pain Ache	Aspirin, Caffeine