NDC 0220-2329

Gratiola officinalis

Gratiola Officinalis

Gratiola officinalis is a Oral Pellet in the Human Otc Drug category. It is labeled and distributed by Boiron. The primary component is Gratiola Officinalis.

• Product ID: 0220-2329_7acfd065-58b7-21f8-e053-2991aa0a252a
• NDC: 0220-2329
• Product Type: Human Otc Drug
• Proprietary Name: Gratiola officinalis
• Generic Name: Gratiola Officinalis
• Dosage Form: Pellet
• Route of Administration: ORAL
• Marketing Start Date: 1983-03-03
• Marketing Category: UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
• Labeler Name: Boiron
• Substance Name: GRATIOLA OFFICINALIS
• Active Ingredient Strength: 30 [hp_C]/30[hp_C]
• NDC Exclude Flag: N
• Listing Certified Through: 2019-12-31

Packaging

NDC 0220-2329-41

30 [hp_C] in 1 TUBE (0220-2329-41)

• Marketing Start Date: 1983-03-03
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 0220-2329-41 [00220232941]

Gratiola officinalis PELLET

• Marketing Category: unapproved homeopathic
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 1983-03-03

Drug Details

Active Ingredients

Ingredient	Strength
GRATIOLA OFFICINALIS	30 [hp_C]/30[hp_C]

OpenFDA Data

• SPL SET ID: 7acfd065-58b6-21f8-e053-2991aa0a252a
• Manufacturer:
  • Boiron
• UNII:
  • BDD9991A36

NDC Crossover Matching brand name "Gratiola officinalis" or generic name "Gratiola Officinalis"

NDC	Brand Name	Generic Name
0220-2329	Gratiola officinalis	GRATIOLA OFFICINALIS
15631-0211	GRATIOLA OFFICINALIS	GRATIOLA OFFICINALIS
68428-947	Gratiola officinalis	GRATIOLA OFFICINALIS
71919-325	Gratiola officinalis	GRATIOLA OFFICINALIS
64117-234	STOMACH CRAMPS	GRATIOLA OFFICINALIS