APOMORPHINUM MURIATICUM
- Product NDC
- 10191-1225
- 11-digit product format
- 101911225
- Labeler code
- 10191
- Product ID
- 10191-1225_1cd90a1d-3598-4430-b7b6-e5406454b2c9
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- APOMORPHINE HYDROCHLORIDE
- Dosage form
- PELLET
- Route
- SUBLINGUAL
- Labeler
- Remedy Makers
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2002-03-18
- Marketing end
- 0000-00-00
- Substance
- APOMORPHINE HYDROCHLORIDE
- Active strength
- 3 [hp_X]/1
- Pharmacologic classes
- Dopamine Agonists [MoA],Dopaminergic Agonist [EPC]
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 10191-1225-2 | APOMORPHINUM MURIATICUM | 153 in 1 VIAL, GLASS | PELLET | 153 | | 6 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 10191-1225 | APOMORPHINUM MURIATICUM (APOMORPHINE HYDROCHLORIDE) PELLET [REMEDY MAKERS] | 6 | Legacy NDC, 1 package rows | 20091231_72093a71-cada-44bc-985e-51e30fd91a1a.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 10191-1225-2 | 10191122502 | 153 in 1 VIAL, GLASS | Historical |