Dicyclomine Hydrochloride
- Product NDC
- 68151-2265
- 11-digit product format
- 681512265
- Labeler code
- 68151
- Product ID
- 68151-2265_313d0ce5-dd49-4540-8fdf-561d57b15a18
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- dicyclomine hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Carilion Materials Management
- Application
- ANDA040319
- Marketing category
- ANDA
- Marketing start
- 1999-11-03
- Marketing end
- 0000-00-00
- Substance
- DICYCLOMINE HYDROCHLORIDE
- Active strength
- 10 mg/1
- Pharmacologic classes
- Anticholinergic [EPC],Cholinergic Antagonists [MoA]
- NDC exclude flag
- E
- Listing certified through
- 2018-12-31
- 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 |
|---|
| 68151-2265-1 | Dicyclomine Hydrochloride | 1 in 1 BLISTER PACK | CAPSULE | 1 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 68151-2265 | DICYCLOMINE HYDROCHLORIDE CAPSULE [CARILION MATERIALS MANAGEMENT] | 2 | Legacy NDC, 1 package rows | 20171227_d0f831a3-5b2f-4e39-af9b-01e2e3c497b3.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 68151-2265-1 | 68151226501 | 1 in 1 BLISTER PACK | Historical |