ADD
- Product NDC
- 44911-0493
- 11-digit product format
- 449110493
- Labeler code
- 44911
- Product ID
- 44911-0493_142a33a4-a7a0-45c7-a77b-c0eee4903fdf
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- GABA (Gamma-Aminobutyric Acid), L-Dopa, Norepinephrine (Bitartrate), Serotonin (Hydrochloride), Adrenocorticotrophin, Anacardium Orientale, Arsenicum Album, Baryta Carbonica, Calcarea Carbonica, Calcarea Phosphorica, Hyoscyamus Niger, Lycopodium Clavatum
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Engergique, Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2019-04-09
- Marketing end
- 0000-00-00
- Substance
- .GAMMA.-AMINOBUTYRIC ACID; LEVODOPA; NOREPINEPHRINE BITARTRATE; SEROTONIN HYDROCHLORIDE; CORTICOTROPIN; ANACARDIUM OCCIDENTALE FRUIT; ARSENIC TRIOXIDE; BARIUM CARBONATE; OYSTER SHELL CALCIUM CARBONATE, CRUDE; TRIBASIC CALCIUM PHOSPHATE; HYOSCYAMUS NIGER; LYCOPODIUM CLAVATUM SPORE; DATURA STRAMONIUM
- Active strength
- 6 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#