Ambra grisea
- Product NDC
- 0220-0221
- 11-digit product format
- 002200221
- Labeler code
- 0220
- Product ID
- 0220-0221_687e64ac-7271-c2b2-e053-2a91aa0a1f4e
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- AMBERGRIS
- Dosage form
- PELLET
- Route
- ORAL
- Labeler
- Boiron
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 1983-03-03
- Marketing end
- 0000-00-00
- Substance
- AMBERGRIS
- Active strength
- 6 [hp_C]/6[hp_C]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record