Mecamylamine Hydrochloride
- Product NDC
- 79739-7183
- 11-digit product format
- 797397183
- Labeler code
- 79739
- Product ID
- 79739-7183_1b79ef78-f4da-49a6-9f36-89b0da19d39b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Mecamylamine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- LGM Pharma Solutions, LLC
- Application
- ANDA204054
- Marketing category
- ANDA
- Marketing start
- 2013-03-19
- Marketing end
- 0000-00-00
- Substance
- MECAMYLAMINE HYDROCHLORIDE
- Active strength
- 3 mg/1
- Pharmacologic classes
- Autonomic Ganglionic Blocker [EPC],Decreased Autonomic Ganglionic Activity [PE]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- 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 |
|---|
| 79739-7183-1 | Mecamylamine Hydrochloride | 100 in 1 BOTTLE | TABLET | 100 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 79739-7183 | MECAMYLAMINE HYDROCHLORIDE TABLET [LGM PHARMA SOLUTIONS, LLC] | 2 | Legacy NDC, 1 package rows | 20240517_1b79ef78-f4da-49a6-9f36-89b0da19d39b.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 79739-7183-1 | 79739718301 | 100 TABLET in 1 BOTTLE (79739-7183-1) | 100 tablet | 2013-03-19 | 0000-00-00 | No | No | Current |