Vecamyl
- Product NDC
- 45043-558
- 11-digit product format
- 450430558
- Labeler code
- 45043
- Product ID
- 45043-558_976f404f-4857-4bad-9a3c-9bf3d5ca9f5b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Mecamylamine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Manchester Pharmaceuticals
- 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
- E
- Listing certified through
- 2018-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 45043-558 | VECAMYL (MECAMYLAMINE HYDROCHLORIDE) TABLET [MANCHESTER PHARMACEUTICALS] | 3 | Legacy NDC | 20150702_c6822ce4-e741-4366-b72a-5f5146354f97.zip |