NDC 0067-2070

NoDoz MAXIMUM STRENGTH ALERTNESS AID

Caffeine

NoDoz MAXIMUM STRENGTH ALERTNESS AID is a Oral Tablet, Coated in the Human Otc Drug category. It is labeled and distributed by Glaxosmithkline Consumer Healthcare Holdings (us) Llc. The primary component is Caffeine.

• Product ID: 0067-2070_89a9d8ce-facb-4476-b2df-3717973a1b10
• NDC: 0067-2070
• Product Type: Human Otc Drug
• Proprietary Name: NoDoz MAXIMUM STRENGTH ALERTNESS AID
• Generic Name: Caffeine
• Dosage Form: Tablet, Coated
• Route of Administration: ORAL
• Marketing Start Date: 2009-12-31
• Marketing End Date: 2019-07-11
• Marketing Category: OTC MONOGRAPH FINAL / OTC MONOGRAPH FINAL
• Application Number: part340
• Labeler Name: GlaxoSmithKline Consumer Healthcare Holdings (US) LLC
• Substance Name: CAFFEINE
• Active Ingredient Strength: 200 mg/1
• NDC Exclude Flag: N

Packaging

NDC 0067-2070-60

1 BOTTLE in 1 CARTON (0067-2070-60) > 60 TABLET, COATED in 1 BOTTLE

• Marketing Start Date: 2009-12-31
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 0067-2070-10 [00067207010]

NoDoz MAXIMUM STRENGTH ALERTNESS AID TABLET, COATED

• Marketing Category: OTC monograph final
• Application Number: part340
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2009-12-31
• Marketing End Date: 2014-12-31

NDC 0067-2070-36 [00067207036]

NoDoz MAXIMUM STRENGTH ALERTNESS AID TABLET, COATED

• Marketing Category: OTC monograph final
• Application Number: part340
• Product Type: HUMAN OTC DRUG
• Billing Unit: EA
• Marketing Start Date: 2009-12-31
• Marketing End Date: 2014-12-31

NDC 0067-2070-16 [00067207016]

NoDoz MAXIMUM STRENGTH ALERTNESS AID TABLET, COATED

• Marketing Category: OTC monograph final
• Application Number: part340
• Product Type: HUMAN OTC DRUG
• Billing Unit: EA
• Marketing Start Date: 2009-12-31
• Marketing End Date: 2014-12-31

NDC 0067-2070-60 [00067207060]

NoDoz MAXIMUM STRENGTH ALERTNESS AID TABLET, COATED

• Marketing Category: OTC monograph final
• Application Number: part340
• Product Type: HUMAN OTC DRUG
• Billing Unit: EA
• Marketing Start Date: 2009-12-31
• Marketing End Date: 2019-07-11

Drug Details

Active Ingredients

Ingredient	Strength
CAFFEINE	200 mg/1

OpenFDA Data

• SPL SET ID: 7ef8b03c-245a-424f-bf75-438559c4418b
• Manufacturer:
  • GlaxoSmithKline Consumer Healthcare Holdings (US) LLC
• UNII:
  • 3G6A5W338E
• RxNorm Concept Unique ID - RxCUI:
  • 198520
  • 795925

NDC Crossover Matching brand name "NoDoz MAXIMUM STRENGTH ALERTNESS AID" or generic name "Caffeine"

NDC	Brand Name	Generic Name
0363-3440	Awake	Caffeine
21130-944	Awake	Caffeine
0363-5009	Caffeine	Caffeine
24385-601	Good Neighbor Pharmacy Stay Awake	Caffeine
0113-0409	good sense stay awake	Caffeine
15579-201	JET ALERT Regular Strength	CAFFEINE
0067-2070	NoDoz	Caffeine
15127-226	Stay Alert	Caffeine
0363-0226	Stay Awake	Caffeine
0904-7955	Stay Awake	Caffeine
11822-0691	Stay Awake	Caffeine
11822-2260	stay awake	caffeine
21130-226	Stay Awake	Caffeine
30142-409	stay awake	Caffeine
30142-726	Stay Awake	Caffeine