Dicyclomine Hydrochloride
- Product NDC
- 70518-0302
- 11-digit product format
- 705180302
- Labeler code
- 70518
- Product ID
- 70518-0302_e7609a03-a2fc-eed1-e053-2a95a90a5074
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Dicyclomine Hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA085082
- Marketing category
- ANDA
- Marketing start
- 2017-03-09
- Marketing end
- 0000-00-00
- Substance
- DICYCLOMINE HYDROCHLORIDE
- Active strength
- 10 mg/1
- Pharmacologic classes
- Anticholinergic [EPC], Cholinergic Antagonists [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-0302-1 | 70518030201 | 60 CAPSULE in 1 BOTTLE, PLASTIC (70518-0302-1) | 60 capsule | 2018-05-16 | 0000-00-00 | No | No | Current |
| 70518-0302-2 | 70518030202 | 30 CAPSULE in 1 BLISTER PACK (70518-0302-2) | 30 capsule | 2018-08-14 | 0000-00-00 | No | No | Current |