Hydrocodone Bitartrate and Acetaminophen
- Product NDC
- 60760-220
- 11-digit product format
- 607600220
- Labeler code
- 60760
- Product ID
- 60760-220_7b205eac-0761-566a-e053-2a91aa0a90d9
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Hydrocodone Bitartrate and Acetaminophen
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- St. Mary's Medical Park Pharmacy
- Application
- ANDA201013
- Marketing category
- ANDA
- Marketing start
- 2012-04-11
- Marketing end
- 0000-00-00
- Substance
- HYDROCODONE BITARTRATE; ACETAMINOPHEN
- Active strength
- 10 mg/1; mg/1
- Pharmacologic classes
- Opioid Agonist [EPC],Opioid Agonists [MoA]
- DEA schedule
- CII
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- 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 |
|---|
| 60760-220-30 | 60760022030 | 30 TABLET in 1 BOTTLE, PLASTIC (60760-220-30) | 30 tablet | 2017-12-04 | 0000-00-00 | No | No | Current |
| 60760-220-60 | 60760022060 | 60 TABLET in 1 BOTTLE, PLASTIC (60760-220-60) | 60 tablet | 2017-12-04 | 0000-00-00 | No | No | Current |
| 60760-220-90 | 60760022090 | 90 TABLET in 1 BOTTLE, PLASTIC (60760-220-90) | 90 tablet | 2017-12-04 | 0000-00-00 | No | No | Current |