Hydrocodone Bitartrate and Acetaminophen
- Product NDC
- 31722-941
- 11-digit product format
- 317220941
- Labeler code
- 31722
- Product ID
- 31722-941_1fb1cd4e-2efd-4893-885a-c05994325955
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Hydrocodone Bitartrate and Acetaminophen
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Camber Pharmaceuticals, Inc.
- Application
- ANDA211487
- Marketing category
- ANDA
- Marketing start
- 2018-11-08
- Marketing end
- 0000-00-00
- Substance
- HYDROCODONE BITARTRATE; ACETAMINOPHEN
- Active strength
- 5 mg/1; mg/1
- Pharmacologic classes
- Opioid Agonist [EPC],Opioid Agonists [MoA]
- DEA schedule
- CII
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 31722-941 | HYDROCODONE BITARTRATE AND ACETAMINOPHEN TABLET [CAMBER PHARMACEUTICALS, INC.] | 6 | Legacy NDC | 20210611_4d5bfd3a-3793-4d24-aedd-c04fa34ea736.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 |
|---|
| 31722-941-01 | 31722094101 | 100 TABLET in 1 BOTTLE (31722-941-01) | 100 tablet | 2018-11-08 | 0000-00-00 | No | No | Current |
| 31722-941-05 | 31722094105 | 500 TABLET in 1 BOTTLE (31722-941-05) | 500 tablet | 2018-11-08 | 0000-00-00 | No | No | Current |