Bethanechol Chloride
- Product NDC
- 62135-756
- 11-digit product format
- 621350756
- Labeler code
- 62135
- Product ID
- 62135-756_0f8f30ff-cd99-1911-e063-6394a90ad218
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Bethanechol Chloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Chartwell RX, LLC
- Application
- ANDA040728
- Marketing category
- ANDA
- Marketing start
- 2007-10-26
- Substance
- BETHANECHOL CHLORIDE
- Active strength
- 10 mg/1
- Pharmacologic classes
- Cholinergic Muscarinic Agonist [EPC], Cholinergic Muscarinic Agonists [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Bethanechol Chloride
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| BETHANECHOL CHLORIDE | 10 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | H4QBZ2LO84 |
| Rxcui | 857321, 857328, 857336, 857340 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 62135-756-12 | Bethanechol Chloride | 120 in 1 BOTTLE | TABLET | 120 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 62135-756 | BETHANECHOL CHLORIDE TABLET [CHARTWELL RX, LLC] | 1 | Current NDC, 1 package rows | 20240123_89267333-ba8b-455b-a8dc-515a888463c2.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 62135-756-12 | 62135075612 | 120 TABLET in 1 BOTTLE (62135-756-12) | 120 tablet | 2024-01-17 | No | No | Historical |