NDC 50332-0108

CETAFEN EXTRA

Acetaminophen

CETAFEN EXTRA is a Oral Tablet in the Human Otc Drug category. It is labeled and distributed by Hart Health. The primary component is Acetaminophen.

• Product ID: 50332-0108_be810cb9-d7f4-481a-808f-527c3a157b29
• NDC: 50332-0108
• Product Type: Human Otc Drug
• Proprietary Name: CETAFEN EXTRA
• Generic Name: Acetaminophen
• Dosage Form: Tablet
• Route of Administration: ORAL
• Marketing Start Date: 1990-01-05
• Marketing Category: OTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL
• Application Number: part343
• Labeler Name: HART Health
• Substance Name: ACETAMINOPHEN
• Active Ingredient Strength: 500 mg/1
• NDC Exclude Flag: E
• Listing Certified Through: 2018-12-31

Packaging

NDC 50332-0108-1

400 PACKET in 1 BOX, UNIT-DOSE (50332-0108-1) > 2 TABLET in 1 PACKET

• Marketing Start Date: 1990-01-05
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 50332-0108-3 [50332010803]

CETAFEN EXTRA TABLET

• Marketing Category: OTC monograph not final
• Application Number: part343
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 1990-01-05
• Inactivation Date: 2020-01-31

NDC 50332-0108-8 [50332010808]

CETAFEN EXTRA TABLET

• Marketing Category: OTC monograph not final
• Application Number: part343
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 1990-01-05
• Inactivation Date: 2020-01-31

NDC 50332-0108-4 [50332010804]

CETAFEN EXTRA TABLET

• Marketing Category: OTC monograph not final
• Application Number: part343
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 1990-01-05
• Inactivation Date: 2020-01-31

NDC 50332-0108-1 [50332010801]

CETAFEN EXTRA TABLET

• Marketing Category: OTC monograph not final
• Application Number: part343
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 1990-01-05
• Inactivation Date: 2020-01-31

NDC 50332-0108-7 [50332010807]

CETAFEN EXTRA TABLET

• Marketing Category: OTC monograph not final
• Application Number: part343
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 1990-01-05
• Inactivation Date: 2020-01-31

Drug Details

Active Ingredients

Ingredient	Strength
ACETAMINOPHEN	500 mg/1

OpenFDA Data

• SPL SET ID: 207cf327-b35c-405c-979e-af25183e6ae5
• Manufacturer:
  • HART Health
• UNII:
  • 362O9ITL9D
• RxNorm Concept Unique ID - RxCUI:
  • 198440
  • 1358835

NDC Crossover Matching brand name "CETAFEN EXTRA" or generic name "Acetaminophen"

NDC	Brand Name	Generic Name
50332-0108	CETAFEN EXTRA	CETAFEN EXTRA
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